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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018220Generated: November 1, 2026

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

https://huagongshe.com/reaction/1018220

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 (1.15g, 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 numberUS06479552B2
Source datasetuspto-grants-2002_11
ORD IDord-51aee2328c3147c7b9d1e7375ac66795
Source noteuspto-grants-2002_11