Veratroyl chloride → HCID 15481278, compound
Reaction equation
[CH2:1]([C:8]1[S:12][C:11]2[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=2[CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:17][O:18][C:19]1[CH:20]=[C:21]([CH:25]=[CH:26][C:27]=1[O:28][CH3:29])[C:22](Cl)=[O:23]>>[CH2:1]([C:8]1[S:12][C:11]2[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=2[C:9]=1[C:22]([C:21]1[CH:25]=[CH:26][C:27]([O:28][CH3:29])=[C:19]([O:18][CH3:17])[CH:20]=1)=[O:23])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
Prepared from 2-benzyl-benzo[b]thiophene and 3,4-dimethoxybenzoyl chloride according to the procedure in Example 8. White solid: MS (EI): [M+], 388.
Sources & evidence
- ORD record
- ord-5e02c8f0fcee4590b591c1b2f4bd3797
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06110962
Reaction notes
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