Trifluoroacetic acid → HCID 86586796, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([NH:14][NH:15]OC(C)(C)C)=[S:11]=C=O)[CH:5]=1.C1(OC)C=CC=CC=1.[C:30]([OH:36])([C:32]([F:35])([F:34])[F:33])=[O:31]>>[F:33][C:32]([F:35])([F:34])[C:30]([OH:36])=[O:31].[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([NH:14][NH2:15])=[S:11])[CH:5]=1Participants
4
Procedure
A solution of 3-(N′-tert-butoxy-carbonyl-hydrazinocarbothioyl)-benzoic acid methyl ester (0.93 g) in TFA (9 mL)/anisole (2 mL) was stirred at 0° C. for 1 h. The solvents were evaporated in vacuum to give crude 3-hydrazinothiocarbonyl-benzoic acid methyl ester trifluoroacetate (0.98 g) as a crystallizing oil.
Workup
- customThe solvents were evaporated in vacuum
Sources & evidence
- ORD record
- ord-eac828648e6d4fcfac7b116cc0e99f1f
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06544985B2
Reaction notes
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