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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372646Generated: October 25, 2026

4-Fluoro-2-methylphenyl isothiocyanate → Methyl (2-(4-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate

https://huagongshe.com/reaction/1372646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-2-methylphenyl isothiocyanateHCID 2737399—
ReactantMethyl (4-amino-2-fluoro-3-hydroxyphenyl)acetateHCID 17859032—
SolventMethanolHCID 887—
ProductMethyl (2-(4-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetateHCID 5877897591%

Reaction Steps

In methanol (30 ml) was dissolved methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate (1.0 g, 5.02 mmol). To the resulting solution was added 4-fluoro-2-methylphenyl isothiocyanate (0.74 ml, 5.23 mmol). After the mixture was stirred at room temperature for 5 days, mercuric oxide (yellow) (1.14 g, 4.36 mmol) was added thereto. The mixture was stirred at 70° C. for 6 hours. After cooling to room temperature, the reaction mixture was filtered through Celite and washed with methanol. The filtrate was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from chloroform/ethyl acetate (30/1) eluate fractions, methyl (2-(4-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate (1.32 g, 91%) was obtained as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-741b8b833de44a6c9572b692b6b7b7c3
Source noteuspto-grants-2007_01