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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | 3-Fluoro-2-methylaniline | HCID 285553 | — |
| Reactant | Methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate | HCID 17859032 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl (2-(3-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate | HCID 44607519 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-23140df8c5754693811589f6f0311bd8 |
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| Source note | uspto-grants-2007_01 |
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