4-Chlorophenyl Isocyanate → HCID 57719838, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH:11]([O:17][CH:18]([CH3:20])[CH3:19])[C:12]([O:14]CC)=[O:13])=[CH:6][C:5]=1[CH2:21][CH2:22][OH:23])[CH3:2].[Cl:24][C:25]1[CH:30]=[CH:29][C:28]([N:31]=[C:32]=[O:33])=[CH:27][CH:26]=1>>[Cl:24][C:25]1[CH:30]=[CH:29][C:28]([NH:31][C:32]([O:23][CH2:22][CH2:21][C:5]2[CH:6]=[C:7]([CH2:10][CH:11]([O:17][CH:18]([CH3:19])[CH3:20])[C:12]([OH:14])=[O:13])[CH:8]=[CH:9][C:4]=2[O:3][CH2:1][CH3:2])=[O:33])=[CH:27][CH:26]=1Participants
3
Procedure
Using ethyl 3-[4-ethoxy-3-(2-hydroxyethyl)phenyl]-2-isopropoxypropanoate and 4-chlorophenylisocyanate, the title compound was obtained in the same manner as described in Example 148.
Sources & evidence
- ORD record
- ord-fb5aaae5c1c3489f8955482160d0a792
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07544835B2
Reaction notes
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