Butyric Acid → HCID 54132859, compound

HRID 484084Notes

Reaction equation

[NH2:1][C:2]1[CH:31]=[CH:30][C:5]([CH:6]=[CH:7][CH2:8][N:9]2[CH2:14][CH2:13][C:12](=[C:15]3[C:21]4[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=4[CH:19]=[CH:18][C:17]4[CH:26]=[CH:27][CH:28]=[CH:29][C:16]3=4)[CH2:11][CH2:10]2)=[CH:4][CH:3]=1.[C:32](O)(=[O:36])[CH2:33][CH2:34][CH3:35]>>[C:32]([NH:1][C:2]1[CH:3]=[CH:4][C:5]([CH:6]=[CH:7][CH2:8][N:9]2[CH2:10][CH2:11][C:12](=[C:15]3[C:16]4[CH:29]=[CH:28][CH:27]=[CH:26][C:17]=4[CH:18]=[CH:19][C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][C:21]3=4)[CH2:13][CH2:14]2)=[CH:30][CH:31]=1)(=[O:36])[CH2:33][CH2:34][CH3:35]

Participants

Reactant 2

HCID 264Butyric Acid

HCID 53692038HCID 53692038, compound2×

Product 1

HCID 54132859HCID 54132859, compoundYield 68.5%

Procedure

This compound was prepared from 1-(4-Aminocinnamyl)-4-(5H-dibenzo[a,d]cyclohepten-5-ylidene)piperidine (compound 5) and butanoic acid. Yield 68.5%

Sources & evidence

ORD record: ord-24da43d7fc94489684c1a91ea9e9edb4
Source dataset: uspto-grants-1993_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05229400

Reaction notes

Loading…