trans-3-(Trifluoromethyl)cinnamoyl chloride → HCID 57841311, compound
Reaction equation
[C:1]([C:11]1[CH:31]=[CH:30][C:14]([CH2:15][NH:16][C:17]2[CH:29]=[CH:28][C:20]3[O:21][C:22]([CH3:27])([CH3:26])[O:23][C:24](=[O:25])[C:19]=3[CH:18]=2)=[CH:13][CH:12]=1)#[C:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[F:32][C:33]([F:46])([F:45])[C:34]1[CH:35]=[C:36](/[CH:40]=[CH:41]/[C:42](Cl)=[O:43])[CH:37]=[CH:38][CH:39]=1>>[C:1]([C:11]1[CH:31]=[CH:30][C:14]([CH2:15][N:16]([C:17]2[CH:29]=[CH:28][C:20]3[O:21][C:22]([CH3:26])([CH3:27])[O:23][C:24](=[O:25])[C:19]=3[CH:18]=2)[C:42](=[O:43])/[CH:41]=[CH:40]/[C:36]2[CH:37]=[CH:38][CH:39]=[C:34]([C:33]([F:45])([F:46])[F:32])[CH:35]=2)=[CH:13][CH:12]=1)#[C:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]Participants
3
Procedure
The title compound was prepared following the procedure E using 6-[(4-dec-1-ynylbenzyl)amino]-2,2-dimethyl-4H-1,3-benzodioxin-4-one and (2E)-3-[3-(trifluoromethyl)phenyl]acryloyl chloride. HPLC, Rt: 6.6 min (purity: 87.4%).
Sources & evidence
- ORD record
- ord-d118cdb2a064483bbcd68d35f59281cf
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07589232B2
Reaction notes
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