Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372648Generated: October 25, 2026

Thiophosgene → Methyl (2-(3-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate

https://huagongshe.com/reaction/1372648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophosgeneHCID 10040—
Reactant3-Fluoro-2-methylanilineHCID 285553—
ReactantMethyl (4-amino-2-fluoro-3-hydroxyphenyl)acetateHCID 17859032—
SolventTetrahydrofuranHCID 8028—
ProductMethyl (2-(3-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetateHCID 4460751973%

Reaction Steps

In THF (20 ml) was dissolved 3-fluoro-2-methylaniline (0.57 ml, 5.0 mmol). To the resulting solution was added thiophosgene (990 mg, 5.0 mmol) under stirring at room temperature. After the reaction mixture was stirred for 4 hours at room temperature, methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate (996 mg, 5.0 mmol) was added thereto. The resulting mixture was stirred further at room temperature for 2 days. Mercuric oxide (yellow) (1.08 g, 5.0 mmol) was added and the mixture was stirred at 70° C. for 4.5 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 n-hexane/ethyl acetate (4/1) eluate fractions, methyl (2-(3-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate (1.21 g, 73%) was obtained as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-23140df8c5754693811589f6f0311bd8
Source noteuspto-grants-2007_01