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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643577Generated: October 30, 2026

Trifluoroacetic acid → HCID 11694142, compound

https://huagongshe.com/reaction/643577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactanttert-Butyl carbamateHCID 77922—
Reactant2-Hydroxy-5-(trifluoromethoxy)benzaldehydeHCID 1268058—
SolventAcetonitrileHCID 6342—
ProductHCID 11694142HCID 11694142—

Reaction Steps

A solution of 5-(trifluoromethoxy)salicylaldehyde (4.85 mmol, 1.0 g), tert-butyl carbamate (14.55 mmol, 1.70 g), triethylsilane (14.55 mmol, 2.3 mL), trifluoroacetic acid (9.7 mmol, 0.72 mL) in acetonitrile was stirred at room temperature overnight. The reaction was quenched with saturated NaHCO3 and extracted with EtOAc. The combined organic layers were dried over Na2SO4 and purified by silica gel chromatography (15%-100% EtOAc/hexane). The resulting yellow solid was then dissolved in a mixture of TFA (10 mL) and dichloromethane (20 mL) and stirred for 2 hours at room temperature. The volatile solvents were then removed by rotovap to afford 2-(aminomethyl)-4-(trifluoromethoxy)phenol as a yellow oil. 1H NMR (CD3OD) 7.28 (s, 1H), 7.22 (m, 1H), 6.97 (m, 1H), 4.13 (s, 2H), 1.59 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700591B2
Source datasetuspto-grants-2010_04
ORD IDord-8455746be98448b09a0da6c48299ad3d
Source noteuspto-grants-2010_04