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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522780Generated: November 3, 2026

HCID 89444805, compound → HCID 89444767, compound

https://huagongshe.com/reaction/1522780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 89444805HCID 89444805—
SolventAnilineHCID 6115—
ProductHCID 89444767HCID 8944476777.1%

Reaction Steps

A solution of 4-[3-Acetylsulfanyl-4,4,4-trifluoro-3-(3,4,5-trichloro-phenyl)-butyryl]-2-methyl-benzoic acid tert-butyl ester (1.33 g) in aniline (13 mL) was stirred at room temperature for 3 hours. The mixture was quenched with a solution of hydrochloric acid (1N), extracted with ethyl acetate and washed with brine. The collected organic phases were dried over magnesium sulfate, filtered and the filtrate was evaporated under vacuo. The residue was purified by chromatography on silica gel (eluent: cyclohexane/dichloromethane) to give 2-Methyl-4-[4,4,4-trifluoro-3-mercapto-3-(3,4,5-trichloro-phenyl)-butyryl]-benzoic acid tert-butyl ester (950 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09078444B2
Source datasetuspto-grants-2015_07
ORD IDord-a291e730eb1a44438741d886c5f98f23
Source noteuspto-grants-2015_07