Ethyl Thioglycolate → Ethyl (2,4,6-trimethylbenzylthio)acetate
反応式
CC1C=CC(C[S:7][CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=CC=1.[CH3:16][C:17]1[CH:24]=[C:23]([CH3:25])[CH:22]=[C:21]([CH3:26])[C:18]=1[CH2:19]Cl.CC[O-].[Na+].SCC(OCC)=O>C(O)C>[CH3:16][C:17]1[CH:24]=[C:23]([CH3:25])[CH:22]=[C:21]([CH3:26])[C:18]=1[CH2:19][S:7][CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10]参加物
6
実験手順
The procedure is as in Example 29 for the preparation of ethyl (4-methylbenzylthio)acetate, starting with 2,4,6-trimethylbenzyl chloride (10.25 g), a 2M ethanolic solution of sodium ethylate (32.5 cc) and ethyl 2-mercaptoacetate (7.1 g) in ethanol (150 cc). Ethyl (2,4,6-trimethylbenzylthio)acetate (11 g) is thereby obtained, and is used in the crude state in the subsequent syntheses.
出典と根拠
- ORDレコード
- ord-0b4f86ca9aad415e95eaf1a57bbf8fb7
- 出典データセット
- uspto-grants-1989_12
- 特許番号
- US04886835
反応ノート
読み込み中…