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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-(trifluoromethyl)phenolHCID 120246—
Reactant2-Chloro-1,1,1-triethoxyethaneHCID 305922—
SolventAcetic AcidHCID 176—
Product2-ChloroMethyl-5-trifluoroMethyl-benzooxazoleHCID 1513375177%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249102B2
Source datasetuspto-grants-2016_02
ORD IDord-461639f1df16415685603abe2b8a8c9c
Source noteuspto-grants-2016_02