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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372642Generated: October 25, 2026

5-Chloro-2-methylphenyl isothiocyanate → Methyl (2-(5-chloro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate

https://huagongshe.com/reaction/1372642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-methylphenyl isothiocyanateHCID 29519—
ReactantMethyl (4-amino-2-fluoro-3-hydroxyphenyl)acetateHCID 17859032—
SolventMethanolHCID 887—
ProductMethyl (2-(5-chloro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetateHCID 58778453104.6%

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 5-chloro-2-methylphenyl isothiocyanate (0.674 ml, 4.58 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 resulting 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, v/v) eluate fractions, methyl (2-(5-chloro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate (1.67 g, 100%) was obtained as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-872731dd92f545cd9cb6dcde9122e441
Source noteuspto-grants-2007_01