Ethanol → HCID 11264629, compound
Reaction equation
[C:1]1([C:11](=[CH2:15])[C:12]([OH:14])=[O:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.S(=O)(=O)(O)O.[CH2:21](O)[CH3:22]>>[CH2:21]([O:13][C:12](=[O:14])[C:11]([C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1)=[CH2:15])[CH3:22]Participants
4
Procedure
1-Naphthylacrylic acid (9.5 g), conc. sulfuric acid (1 ml) and ethanol (100 ml) were subjected to reaction and post-treatment in a similar manner to that described in Reference example 10(a) to obtain the title compound (10.2 g, 94%) as a colorless oil.
Sources & evidence
- ORD record
- ord-29fd3b5174fc4327a949bffebbcbd500
- Source dataset
- uspto-grants-1999_12
- Patent number
- US06005116
Reaction notes
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