Allyl bromide → 2-allyloxy-N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-3-p-tolyl-propionamide
반응식
[CH2:1](Br)[CH:2]=[CH2:3].[OH:5][CH:6]([CH2:24][C:25]1[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=1)[C:7]([NH:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][C:15]([O:18][CH2:19][C:20]#[CH:21])=[C:14]([O:22][CH3:23])[CH:13]=1)=[O:8].[OH-].[Na+]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.ClCCl>[CH2:1]([O:5][CH:6]([CH2:24][C:25]1[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=1)[C:7]([NH:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][C:15]([O:18][CH2:19][C:20]#[CH:21])=[C:14]([O:22][CH3:23])[CH:13]=1)=[O:8])[CH:2]=[CH2:3]참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
Allyl bromide (1.2 g, 10 mmol) is added slowly at room temperature to a mixture of 2-hydroxy-N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-3-p-tolyl-propionamide (3.0 g, 8.2 mmol), 30% sodium hydroxide solution (6.5 ml, 41 mmol) and catalytic amounts of tetrabutylammonium bromide (50 mg) in 30 ml of dichloromethane. The reaction is stirred for 16 hours at +40° C. Subsequently the mixture is evaporated and the residue is diluted with water and dichloromethane. The phases are separated and the aqueous phase is extracted three times with dichloromethane. The combined organic layer is washed with brine, dried over sodium sulfate and evaporated. The remaining oil is purified by chromatography on silica gel (ethyl acetate/hexane 1:1) to give 2-allyloxy-N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-3-p-tolyl-propionamide (E1.17).
후처리
- customSubsequently the mixture is evaporated
- additionthe residue is diluted with water and dichloromethane
- customThe phases are separated
- extractionthe aqueous phase is extracted three times with dichloromethane
- washThe combined organic layer is washed with brine
- dry with materialdried over sodium sulfate
- customevaporated
- customThe remaining oil is purified by chromatography on silica gel (ethyl acetate/hexane 1:1)
출처 및 근거
- ORD 기록
- ord-7b2d5379a07e4769a2a07c0e199e8ffc
- 출처 데이터셋
- uspto-grants-2010_04
- 특허 번호
- US07700522B2
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