HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772284Generated: November 1, 2026
2-Amino-4-(trifluoromethyl)phenol → 2-ChloroMethyl-5-trifluoroMethyl-benzooxazole
https://huagongshe.com/reaction/1772284
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-4-(trifluoromethyl)phenol | HCID 120246 | — |
| Reactant | 2-Chloro-1,1,1-triethoxyethane | HCID 305922 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-ChloroMethyl-5-trifluoroMethyl-benzooxazole | HCID 15133751 | 77% |
Reaction Steps
2-Chloro-1,1,1-triethoxyethane (410 μL, 2.15 mmol) was added to a suspension of 2-amino-4-trifluoromethylphenol (370 mg, 1.79 mmol) in acetic acid (7 mL); during the addition the solution began to clear. The solution was heated at 120° C. (external temperature). After three hours the reaction mixture was cooled and the volatiles were removed under reduced pressure. Purification by silica gel chromatography, eluting with a gradient of 0 to 10% ethyl acetate in heptanes, gave 2-chloromethyl-5-trifluoromethyl-benzoxazole as a yellow oil (324 mg, 77%). (CI, m/z): [M+H]+ 236; 1H NMR (CDCl3): δ 8.05 (s, 1H), 7.66-7.73 (m, 2H), 4.79 (s, 2H); 19F NMR (376 MHz, CDCl3): δ ppm −61.26 (s, 3F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249102B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-461639f1df16415685603abe2b8a8c9c |
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| Source note | uspto-grants-2016_02 |
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