HCID 44220286, compound → HCID 45267625, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8](/[C:10](/[C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:11]\[C:12]([O:14]CC)=[O:13])=[CH:7][C:6]=2[CH:23]=1.CC1C=CC2OC(/C(/C3C=CC=CC=3)=C/C(OCC)=O)=CC=2C=1.CC1C=CC2OC(/C(/C3C=CC=CC=3)=C\C(O)=O)=CC=2C=1>>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8](/[C:10](/[C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:11]/[C:12]([OH:14])=[O:13])=[CH:7][C:6]=2[CH:23]=1Participants
4
Procedure
By a procedure similar to that of example 1.85.4, starting from a mixture of (Z)-ethyl 3-(5-methyl-2-benzofuranyl)-3-phenylacrylate and (E)-ethyl 3-(5-methyl-2-benzofuranyl)-3-phenylacrylate, a mixture of (Z)-3-(5-methyl-2-benzofuranyl)-3-phenylacrylic acid and (E)-3-(5-methyl-2-benzofuranyl)-3-phenylacrylic acid was obtained as yellowish solid.
Sources & evidence
- ORD record
- ord-8e71981caf304fd7ba0a78aa2b154be8
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
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