2-(4-chlorophenyl)ethenesulfonyl Chloride → Ethyl 2-{4-[2-(4-chlorostyrenesulphonylamino)-ethyl]-phenoxy}-2-methylpropionate
Reaction equation
[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([CH:6]=[CH:7][S:8](Cl)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[NH2:14][CH2:15][CH2:16][C:17]1[CH:31]=[CH:30][C:20]([O:21][C:22]([CH3:29])([CH3:28])[C:23]([O:25][CH2:26][CH3:27])=[O:24])=[CH:19][CH:18]=1>>[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([CH:6]=[CH:7][S:8]([NH:14][CH2:15][CH2:16][C:17]2[CH:18]=[CH:19][C:20]([O:21][C:22]([CH3:28])([CH3:29])[C:23]([O:25][CH2:26][CH3:27])=[O:24])=[CH:30][CH:31]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1Participants
3
Procedure
From p-chlorostyrenesulphonyl chloride and ethyl 2-[4-(2-aminoethyl)-phenoxy]-2-methylpropionate; colourless oil, nD20 =1.5625;
Sources & evidence
- ORD record
- ord-69f4a1eb8a4f4684913a4dea7432d1fc
- Source dataset
- uspto-grants-1981_03
- Patent number
- US04258058
Reaction notes
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