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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278889Generated: October 25, 2026

Trifluoroacetic acid → (S)-3-(4-benzyloxy-phenyl)-N1,N1-diethyl-propane-1,2-diamine

https://huagongshe.com/reaction/278889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant[2-(4-Benzyloxy-phenyl)-1-(diethylamino-methyl)-ethyl]-carbamic acid tert-butyl esterHCID 18711795—
SolventDichloromethaneHCID 6344—
Product(S)-3-(4-benzyloxy-phenyl)-N1,N1-diethyl-propane-1,2-diamineHCID 5997335890%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 171 mg (0.4 mmol) [2-(4-benzyloxy-phenyl)-1-(diethylamino-methyl)-ethyl]-carbamic acid tert-butyl ester in 2 mL dichloromethane was treated with 0.5 mL 2,2,2-triflouroacetic acid and the resulting solution stirred 3 hours at 25° C. The mixture was concentrated at reduced pressure to a viscous amber oil to which was added 30 mL saturated aqueous sodium bicarbonate solution and the resulting mixture extracted with three 20 mL portions of ethyl acetate. The combined extracts were washed with two 50 mL portions of brine, dried over anhydrous sodium sulfate, and concentrated at reduced pressure and the residue purified by column chromatography using ethyl acetate containing 1% methanol as eluent. There was obtained 112 mg (90%) of (S)-3-(4-benzyloxy-phenyl)-N1,N1-diethyl-propane-1,2-diamine as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362174B1
Source datasetuspto-grants-2002_03
ORD IDord-74d4c9ba9b954a1082f57be9e3135433
Source noteuspto-grants-2002_03