2-benzoyl-5-chlorobenzofuran → HCID 44222632, compound
Reaction equation
C(C1OC2C=CC(Cl)=CC=2C=1)(=O)C1C=CC=CC=1.[Cl:19][C:20]1[CH:21]=[CH:22][C:23]2[O:27][C:26](/[C:28](/[C:35]3[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=3)=[CH:29]\[C:30]([O:32][CH2:33][CH3:34])=[O:31])=[CH:25][C:24]=2[CH:41]=1>>[Cl:19][C:20]1[CH:21]=[CH:22][C:23]2[O:27][C:26](/[C:28](/[C:35]3[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=3)=[CH:29]/[C:30]([O:32][CH2:33][CH3:34])=[O:31])=[CH:25][C:24]=2[CH:41]=1Participants
3
Procedure
By a procedure similar to that of example 1.85.3, starting from 2-benzoyl-5-chlorobenzofuran, a mixture of (Z)-ethyl 3-(5-chloro-2-benzofuranyl)-3-phenylacrylate and (E)-ethyl 3-(5-chloro-2-benzofuranyl)-3-phenylacrylate was obtained as yellowish oil.
Sources & evidence
- ORD record
- ord-0067afc7f2f24ff5964031cb5af79734
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
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