반응식
[Br:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].Cl.[OH-].[Na+]>C1COCC1>[Br:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[CH:6][C:3]=1[CH2:4][NH2:5]참가 물질
5
실험 절차
13.9 ml (13.9 mmol) of borane-THF complex (1 M) are provided with ice cooling. Slowly a solution of 604 mg (2.8 mmol) of 2-bromo-4-chlorobenzonitrile (Example 1A) in 60 ml of THF is added. Thereafter the reaction mixture is heated under reflux for 1 h, cooled, and 20 ml of 1N hydrochloric acid are added dropwise with ice cooling. For the work up, the solution is rendered alkaline with a 1N sodium hydroxide solution and extracted with dichloromethane. The organic phase is dried over sodium sulfate and concentrated on a rotary evaporator. The crude product (450 mg, about 73% pure) is reacted further without purification.
후처리
- custom13.9 ml (13.9 mmol) of borane-THF complex (1 M) are provided with ice cooling
- temperatureThereafter the reaction mixture is heated
- temperatureunder reflux for 1 h
- temperaturecooled
- extractionextracted with dichloromethane
- dry with materialThe organic phase is dried over sodium sulfate
- concentrationconcentrated on a rotary evaporator
- customThe crude product (450 mg, about 73% pure) is reacted further without purification
출처 및 근거
- ORD 기록
- ord-97c2bf116a88454bacd6d5bfad9720cd
- 출처 데이터셋
- uspto-grants-2011_07
- 특허 번호
- US07977349B2
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