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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2122147Generated: October 30, 2026

3-(Trifluoromethoxy)benzylamine → 3-[[[3-(Trifluoromethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol

https://huagongshe.com/reaction/2122147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethoxy)benzylamineHCID 145264—
Reactant2-(Trifluoromethyl)oxiraneHCID 520769—
Product3-[[[3-(Trifluoromethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanolHCID 2191877737%

Reaction Conditions

Temperature80 °C

Reaction Steps

EX-632A) 3-Trifluoromethoxybenzenemethanamine (1.15 g, 6 mmol) and 1,1,1-trifluoro-2,3-epoxypropane (0.67 g, 6 mmol) were combined and stirred at 80° C. for 1.5 h. The mixture was cooled to room temperature, and the resulting solid was recrystallized from hot hexanes. The white solid was isolated by vacuum filtration and washed with cold hexanes to give 0.67 g (37%) of pure 3-[[[3-(trifluoromethoxy)-phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol. 1H NMR (CDCl3) δ 7.37 (t, 1H), 7.24 (d, 1H), 7.15 (m, 2H), 3.99 (m, 1H), 3.85 (d, 2H), 2.98 (dd, 1H), 2.88 (dd, 1H), 2.79 (s, 1H). 19F NMR (CDCl3) δ −58.19 (s, 3F), −78.88 (s, 3F). HRMS calcd. for C11H11F6NO2: 304.0772 [M+H]+, found: 304.0794.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696435B2
Source datasetuspto-grants-2004_02
ORD IDord-4c80a3929d3d401abd9ac6b9bb9db72f
Source noteuspto-grants-2004_02