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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48064Generated: October 26, 2026

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

https://huagongshe.com/reaction/48064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethoxy)benzylamineHCID 145264—
Reactant2-(Trifluoromethyl)oxiraneHCID 520769—
Product[[3-(Trifluoromethoxy)-phenyl]methyl]amino-1,1,1-trifluoro-2-propanolHCID 86588363—

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) δ7.37 (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 numberUS06699898B2
Source datasetuspto-grants-2004_03
ORD IDord-05650c13c5504aa0a04f2489809bbca1
Source noteuspto-grants-2004_03