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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069091Generated: November 2, 2026

Ethyl chloroformate → Tert-butyl 3-(hydroxymethyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/2069091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(tert-Butoxycarbonyl)morpholine-3-carboxylic acidHCID 2760133—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-(hydroxymethyl)morpholine-4-carboxylateHCID 505835974.2%

Reaction Steps

Ethyl chlorocarbonate (149 μL; TCI) was added to a THF (8 mL) solution of morpholine-3, 4-dicarboxylic acid 4-tert-butyl ester (300 mg; Ast) and diisopropylethylamine (560 μL; WAKO) with ice cooling and the resulting mixture was stirred at room temperature for 1 and half hours. Sodium tetrahydroborate (197 mg; WAKO) was added at room temperature, the resulting mixture was stirred for 15 minutes followed by the addition of methanol (1.2 mL) with ice cooling, and the resulting mixture was stirred at room temperature for 2 hours. The reaction mixture solution was concentrated under reduced pressure, ethyl acetate and saturated aqueous sodium bicarbonate solution were added to extract the reaction mixture, then the organic layer was dried, and the solvent was evaporated under reduced pressure to give the title compound (209 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299055B2
Source datasetuspto-grants-2012_10
ORD IDord-d33858a942ae4b9bbd474c7030ef636b
Source noteuspto-grants-2012_10