溴化
醇 → 溴代烷:查看反应物、产物、反应条件与来源依据,探索相关转化和合成路径。
- 试剂
- KBr 与 50% H2SO4 水溶液
- 条件
- 加热回流,随后蒸出溴代烷
- 反应类别
- 卤化
- 方程式
- R-OH + HBr -> R-Br + H2O
概览
在溴化物和酸的作用下,醇转化为溴代烷。
转化
- 方程式
- R-OH + HBr -> R-Br + H2O
- 试剂
- KBr 与 50% H2SO4 水溶液
- 反应环境
- 加热回流,随后蒸出溴代烷
- 反应类别
- 卤化
- 机理
- 卤化
- Evidence level
- 教材核心内容
参考步骤
Reference preparation: 1-bromobutane
1-丁醇 → 1-溴丁烷
物料与用量
- Sodium bromide — 10 g
- Water — 10 cm³
- Butan-1-ol — 7.5 cm³
- Concentrated sulfuric acid — 10 cm³, added slowly
- Concentrated hydrochloric acid — wash
- Dilute sodium carbonate solution — wash
仪器装置
- Round-bottom flask
- Large cold-water bath
- Vertical condenser
- Tap funnel
- Distillation head and receiver
- 分液漏斗
- Electric heat source
实验步骤
- Place sodium bromide, water and butan-1-ol in the flask and partially immerse the flask in a cold-water bath.
- Fit a vertical condenser and tap funnel. Add the concentrated sulfuric acid slowly through the tap funnel while gently shaking and maintaining external cooling.
- Remove the tap funnel and cold-water bath, then heat the mixture gently under reflux for about 45 minutes.
- Stop heating, allow the apparatus to cool, then rearrange it for distillation and collect the 1-bromobutane/water distillate.
后处理与分离
- Separate the 1-bromobutane layer from water.
- Wash the organic layer with concentrated hydrochloric acid to remove unreacted butan-1-ol.
- Wash with dilute sodium carbonate solution, venting frequently because carbon dioxide is produced.
- Dry the organic layer and redistil using an appropriate boiling-range cut if a purified sample is required.
关键控制条件
- The acid addition is exothermic: add slowly with cooling; do not charge all acid at once.
- Use a fume cupboard, eye protection and an electric heat source; the organic materials are volatile and flammable.
- Confirm which separating-funnel layer contains 1-bromobutane from density data rather than assuming it is the upper layer.
实验技术
Reflux setup
Boil the reaction while returning condensed vapour to the same flask, so volatile material is not continuously lost.
装置设置
- Charge the flask before fitting the condenser; do not fill the flask more than about half full.
- Run cooling water into the lower condenser inlet and out from the upper outlet.
- Keep the top of an ordinary reflux condenser open to the atmosphere unless the cited procedure specifies a pressure-rated closed system.
- Heat to a gentle, steady boil so the condensation line remains within the condenser and liquid returns continuously to the flask.
操作检查
- Use an electric bath or mantle for flammable organic liquids; do not use a naked flame.
- Start condenser water before heating and confirm that hoses are secure.
- If addition is exothermic, complete the controlled addition and cooling stage before sustained reflux.
Distillation setup
Rearrange the apparatus to collect a volatile product or fraction instead of returning condensate to the reaction flask.
装置设置
- Position the thermometer bulb at the entrance to the condenser so it measures vapour entering the condenser.
- Run cooling water into the lower condenser connection and out through the upper connection.
- Heat gradually and collect only the fraction specified by the cited boiling range or procedure.
操作检查
- Do not distil a flask to dryness.
- Use an electric heat source for flammable mixtures.
- Change from reflux to distillation only after heating has stopped and the apparatus has cooled enough to handle safely.
Liquid–liquid work-up
Separate the organic product layer from the aqueous reaction mixture, then wash and dry it before final purification.
装置设置
- Identify which layer contains the product from density data or a small drop test; do not assume the organic layer is always on top.
- Invert gently during washing and vent frequently away from people, especially when carbonate wash produces carbon dioxide.
- Drain and retain both layers until product identity has been confirmed.
- Dry the isolated organic layer until the drying agent remains free-flowing, then decant or filter before final distillation.
操作检查
- Remove the stopper before draining through the tap.
- Release pressure after each inversion during gas-forming washes.
- Record which layer was retained at every wash.
Drying an organic liquid
Remove residual water from a separated organic layer with a compatible anhydrous drying agent.
装置设置
- Remove visible aqueous liquid before treating the organic phase.
- Mix with small portions of drying agent, allow contact and separate the clear liquid from the solid before final purification.
操作检查
- Choose the agent for the product: a drying agent must not react with or strongly retain it.
- Drying removes water, not dissolved organic impurities; boiling-range or spectroscopic checks are still needed.
底物范围
- 适用范围
- Alcohols can be converted into bromoalkanes under bromide and acid conditions that generate hydrogen bromide in situ.
- 来源说明
- Hydrogen bromide is generated in situ. The sulfuric acid is kept at about 50% because concentrated sulfuric acid oxidises some bromide ions to bromine; downstream substitution and elimination are tracked separately.
相关反应
- Chlorination: Alcohols → Chloroalkanes
醇可转化为氯代烷,为后续取代反应引入更易离去的基团。
- Chlorination with thionyl chloride: Alcohols → Chloroalkanes
氯化亚砜将醇转化为氯代烷,同时生成二氧化硫和氯化氢。
- Iodination: Alcohols → Iodoalkanes
在碘和红磷的作用下,醇转化为碘代烷。
- Hydrobromination: Alkenes → Bromoalkanes
溴化氢在烯烃双键两端加成,可生成溴代烷。
- Hydrolysis: Chloroalkanes → Alcohols
氢氧根可取代 C-Cl 中的氯,形成醇。
- Cyanation: Bromoalkanes → Nitriles
氰根取代生成腈,使碳链增加一个碳原子。
- Amination: Bromoalkanes → Amines
氨取代溴,形成伯胺;过量氨可限制进一步烷基化。
- Hydrolysis: Bromoalkanes → Alcohols
氢氧根可取代 C-Br 中的溴,形成醇。
- Hydrolysis: Iodoalkanes → Alcohols
氢氧根可取代 C-I 中的碘,形成醇。
- Elimination: Bromoalkanes → Alkenes
碱促进的消去反应脱去 HBr,生成烯烃。
- Oxidation: Alcohols → Aldehydes
伯醇经受控氧化可生成醛。
- Oxidation: Alcohols → Ketones
仲醇氧化生成酮。
- Oxidation: Alcohols → Carboxylic acids
伯醇充分氧化生成羧酸。
- Free radical bromination: Alkanes → Bromoalkanes
光化学溴化可将烷烃转化为溴代烷。
- Hydration: Alkenes → Alcohols
催化水合将烯烃转化为醇。
- Dehydration: Alcohols → Alkenes
脱水将醇转化为烯烃。
参考文献
- Pearson Edexcel Level 3 Advanced GCE in Chemistry specificationPearson Education Limited · Pearson qualifications · 2024
Supports the textbook-core organic reaction routes used for displayed route and mechanism content.
- Pearson International Advanced Level Chemistry Unit 3B: preparation of 1-bromobutanePearson Education Limited · Pearson qualifications · 2015
Provides the stated quantities, addition order, reflux time, distillation and wash sequence for the 1-bromobutane reference preparation.
- Pearson Edexcel International Advanced Level Chemistry Student Practical GuidePearson Education Limited · Pearson qualifications · 2018
Supports the practical distinctions between reflux, distillation, liquid-liquid separation, washing and drying in organic preparations.
- Reflux and distillation – practical videosRoyal Society of Chemistry · RSC Education
Explains the different purposes and apparatus arrangements for reflux and distillation, including organic preparation and work-up.