Methyl cyanoacetate → HCID 70981646, compound
Reaction equation
[OH:1][N:2]=[C:3](Cl)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[O:10][C:11]([F:14])([F:13])[F:12].[CH3:16][O:17][C:18](=[O:22])[CH2:19][C:20]#[N:21].C[O-].[Na+]>CO>[NH2:21][C:20]1[O:1][N:2]=[C:3]([C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=2[O:10][C:11]([F:14])([F:13])[F:12])[C:19]=1[C:18]([O:17][CH3:16])=[O:22]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In a similar manner as described in Preparation Example 17, by using methanol (160 mL), N-hydroxy-2-(trifluoromethoxy)benzimidoylchloride (8.00 g, 33.39 mmol), methylcyanoacetate (4.31 g, 43.41 mmol) and sodium methoxide (3.61 g, 66.78 mmol), a white solid required compound (9.07 g, 30.02 mmol, 90%) was obtained.
Workup
- customIn a similar manner as described in Preparation Example 17
Sources & evidence
- ORD record
- ord-ffd81fabaac446f8bd0dccf47120c6de
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09132126B2
Reaction notes
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