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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278884Generated: October 26, 2026

Trifluoroacetic acid → (S)-2-(4-benzyloxy-phenyl)-1-morpholin-4-ylmethyl-ethylamine

https://huagongshe.com/reaction/278884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant[2-(4-Benzyloxy-phenyl)-1-morpholin-4-ylmethyl-ethyl]-carbamic acid tert-butyl esterHCID 18711796—
SolventDichloromethaneHCID 6344—
Product(S)-2-(4-benzyloxy-phenyl)-1-morpholin-4-ylmethyl-ethylamineHCID 7009060377%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 1.41 g (3.3 mmol) [2-(4-benzyloxy-phenyl)-1-morpholin-4-ylmethyl-ethyl]-carbamic acid tert-butyl ester in 5 mL dichloromethane was treated with 1.5 mL 2,2,2-triflouroacetic acid and the resulting solution stirred 16 hours at 25° C. The mixture was concentrated at reduced pressure to a viscous amber oil to which was added 50 mL saturated aqueous sodium bicarbonate solution and the resulting mixture extracted with three 50 mL portions of ethyl acetate. The combined extracts were washed with 100 mL brine, dried over anhydrous sodium sulfate and concentrated at reduced pressure affording a soft solid, that was recrystallized from 2,2,4-trimethylpentane containing about 5% ethyl acetate to afford 804 mg (77%) of (S)-2-(4-benzyloxy-phenyl)-1-morpholin-4-ylmethyl-ethylamine as light tan crystals; mp 180-182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362174B1
Source datasetuspto-grants-2002_03
ORD IDord-3b14684ea8bb43219de746122024e37f
Source noteuspto-grants-2002_03