Ethyl bromoacetate → Ethyl [(prop-2-en-1-yl)sulfanyl]acetate
반응식
[C:1]1([CH2:7][C:8](OCC)=[S:9])C=CC=CC=1.Br[CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16].C(S)C=C>CC[O-].[Na+]>[CH2:8]([S:9][CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH:7]=[CH2:1]참가 물질
5
실험 절차
The procedure is as in Example 2 for the preparation of ethyl phenylthioacetate, starting with ethyl bromoacetate (16.7 g), a 2M ethanolic solution of sodium ethylate (50 cc) and allylmercaptan (7.7 cc). After purification by chromatography on a silica column with cyclohexane as eluent, ethyl (allylthio)acetate (3.1 g) is obtained, and is used in the crude state in the subsequent phases.
후처리
- customAfter purification by chromatography on a silica column with cyclohexane as eluent
출처 및 근거
- ORD 기록
- ord-4edc44a1b27942f6856ea2c58b4d1eab
- 출처 데이터셋
- uspto-grants-1989_12
- 특허 번호
- US04886835
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