HCID 22401172, compound → HCID 22401155, compound
Reaction equation
C(OC1C=CC(C=CC(OCC=C)=O)=CC=1[N+]([O-])=O)C=C.[CH2:22]([O:25][C:26]1[CH:31]=[CH:30][C:29]([CH2:32][C:33]([O:35][CH2:36][CH:37]=[CH2:38])=[O:34])=[CH:28][C:27]=1[N+:39]([O-])=O)[CH:23]=[CH2:24]>>[CH2:22]([O:25][C:26]1[CH:31]=[CH:30][C:29]([CH2:32][C:33]([O:35][CH2:36][CH:37]=[CH2:38])=[O:34])=[CH:28][C:27]=1[NH2:39])[CH:23]=[CH2:24]Participants
3
Procedure
Allyl 4-allyloxy-3-nitrocinnamate was reduced by the method described in example 1 using allyl 4-allyloxy-3-nitrophenylacetate in place of allyl 3-nitrocinnamate, to give allyl 4-allyloxy-3-aminophenylacetate.
Sources & evidence
- ORD record
- ord-670604e08b564c5a845c35fd9862e2cf
- Source dataset
- uspto-grants-1996_06
- Patent number
- US05527791
Reaction notes
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