Chlorophenyl isocyanate → HCID 57719934, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:19]=[CH:18][C:7]([CH2:8][CH:9]([C:14]([O:16][CH3:17])=[O:15])[C:10]([O:12][CH3:13])=[O:11])=[CH:6][C:5]=1[CH2:20][OH:21])[CH3:2].[Cl:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[N:29]=[C:30]=[O:31]>>[Cl:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[NH:29][C:30]([O:21][CH2:20][C:5]1[CH:6]=[C:7]([CH:18]=[CH:19][C:4]=1[O:3][CH2:1][CH3:2])[CH2:8][CH:9]([C:14]([O:16][CH3:17])=[O:15])[C:10]([O:12][CH3:13])=[O:11])=[O:31]Participants
3
Procedure
Using dimethyl 2-[4-ethoxy-3-(hydroxymethyl)benzyl]-malonate and 2-chlorophenylisocyanate, the title compound was obtained in the same manner as described in Example 192b).
Sources & evidence
- ORD record
- ord-77b0c904e8a84f54b0c413d3f75700b6
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07544835B2
Reaction notes
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