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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Chloro-2-methylphenyl isothiocyanate | HCID 29519 | — |
| Reactant | Methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate | HCID 17859032 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl (2-(5-chloro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate | HCID 58778453 | 104.6% |
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
| 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-872731dd92f545cd9cb6dcde9122e441 |
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| Source note | uspto-grants-2007_01 |
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