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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307418Generated: October 25, 2026

Morpholine → [1-(3-Morpholin-4-yl-phenyl)ethyl]carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2307418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTrifluoro-methanesulfonic acid 3-(1-tert-butoxycarbonylaminoethyl)phenyl esterHCID 86589152—
SolventDichloromethaneHCID 6344—
Product[1-(3-Morpholin-4-yl-phenyl)ethyl]carbamic acid tert-butyl esterHCID 69850623153.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of trifluoro-methanesulfonic acid 3-(1-tert-butoxycarbonylaminoethyl)phenyl ester (1.5 g, 4.08 mmol), morpholine (8 mL) Pd2(dba)3 (187 mg, 5 mol %), di-t-butyl-biphenylphosphine (243 mg, 20 mol %), potassium phosphate (1.21 g, 5.71 mmol) was stirred at 80° C. in a sealed tube for 10 hours. After cooling down, the reaction mixture was diluted with dichloromethane (50 mL) and washed with water (10 mL). The aqueous layer was extracted with dichloromethane (2×15 mL) and the combined organic layer was dried over magnesium sulfate and concentrated under vacuum. The crude product was purified by flash chromatography of Biotage with 30% ethyl acetate/hexanes to provide the title compound as a pale yellow solid (1.01 g, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831080B2
Source datasetuspto-grants-2004_12
ORD IDord-bc23ea6c09be49498922e6282e198ea3
Source noteuspto-grants-2004_12