HCID 21137946, compound → HCID 21525989, compound
Reaction equation
C([S-])=S.[Na+].[C:5]([S-:8])(=[S:7])[CH3:6].[Na+].C(S[CH:13]([CH2:19][CH2:20][C:21]1[CH:26]=[CH:25][C:24]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[Cl:33])=[CH:23][CH:22]=1)[C:14]([O:16][CH2:17][CH3:18])=[O:15])=S>>[C:5]([S:8][CH:13]([CH2:19][CH2:20][C:21]1[CH:26]=[CH:25][C:24]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[Cl:33])=[CH:23][CH:22]=1)[C:14]([O:16][CH2:17][CH3:18])=[O:15])(=[S:7])[CH3:6]Participants
4
Procedure
When sodium dithioformate is used in the above procedure in place of sodium dithioactate then the product prepared is ethyl α-thioformylthio-γ-(2'-chloro-4-biphenylyl)butyrate.
Workup
- customthe product prepared
Sources & evidence
- ORD record
- ord-edd0e0e097e74ac3ab1595827c3788b7
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03966801
Reaction notes
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