HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814674Generated: November 2, 2026
Hydrochloric Acid → 2-(5-Isocyanato-2-trifluoromethoxyphenyl)benzoxazole
https://huagongshe.com/reaction/1814674
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | 3-(2-Benzoxazolyl)-4-(trifluoromethoxy)benzenamine | HCID 22502044 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(5-Isocyanato-2-trifluoromethoxyphenyl)benzoxazole | HCID 22501949 | 70.4% |
Reaction Steps
A solution of 3-benzoxazol-2-yl-4-trifluoromethoxyphenylamine (210 mg, 0.71 mmol) in 5 mL of dry toluene was stirred while 1.15 mL of 3.1N hydrochloric acid in ethyl acetate was added. The precipitate was concentrated by evaporation. Another 5 mL of toluene was added followed by evaporation. This procedure was repeated 3 times to remove excess of hydrochloric acid. The amine hydrochloride was dissolved in 5 mL of toluene and trichloromethyl chloroformate (0.853 mL, 7.1 mmol) was added. The mixture was refluxed overnight under a nitrogen atmosphere, evaporated at 70° C. followed by stripping with dry toluene. 2-(5-Isocyanato-2-trifluoromethoxyphenyl)benzoxazole (160 mg, 70%) was obtained as crystals and used immediately to synthesize the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875760B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-be8e2e9c2ff5452d9ffa8d59ade9057f |
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| Source note | uspto-grants-2005_04 |
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