Water → HCID 86620812, compound
Reaction equation
[K].[C:2]([O:6][C:7](=[O:13])[CH:8]([C:11]#[N:12])[CH:9]=[O:10])([CH3:5])([CH3:4])[CH3:3].[Cl-].[C:15]1([S+:21]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.O>>[C:28]1([S+:21]([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1.[C:2]([O:6][C:7](=[O:13])[CH:8]([C:11]#[N:12])[CH:9]=[O:10])([CH3:5])([CH3:3])[CH3:4]Participants
5
Procedure
COMP CD-8 was prepared similar to COMP CD-7 at 79% yield from potassium salt of 3-oxo-2-cyanopropanoic acid t-butyl ester (2.07 g, 10 mmol) and 50% solution of triphenylsulfonium chloride in water (5.96 g, 10 mmol) as a yellow color, light weight (fluffy) crystalline material.
Sources & evidence
- ORD record
- ord-038bffab496c45838222c722c8aba08d
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07482113B2
Reaction notes
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