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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057748Generated: October 27, 2026

4-Methylmorpholine → (1S)-[1-Hydroxymethyl-3-(tritylcarbamoyl)propyl]carbamic Acid Benzyl Ester

https://huagongshe.com/reaction/1057748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium borohydrideHCID 4311764—
ReactantZ-Gln(Trt)-OHHCID 10962399—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(1S)-[1-Hydroxymethyl-3-(tritylcarbamoyl)propyl]carbamic Acid Benzyl EsterHCID 10505827—

Reaction Conditions

Temperature23 °C

Reaction Steps

4-Methylmorpholine (1.89 mL, 17.2 mmol, 1 equiv) and ethyl chloroformate (1.65 mL, 17.3 mmol, 1 equiv) were added to a mixture of commercially available Cbz-Gln(Trt)-OH (9.00 g, 17.2 mmol, 1 equiv) in THF (23 mL) at −10° C. After stirring 20 min, the reaction mixture was filtered and the filtrate was added dropwise to a suspension of NaBH4 (1.47 g, 38.9 mmol, 2.25 equiv) in H2O (10 mL) at 0° C. The resulting mixture was allowed to warm to 23° C. and stirred for 5 h. It was then cooled again to 0° C., quenched by the careful addition of 1 N HCl (30 mL) and then partitioned between MTBE (500 mL) and brine (2×100 mL). The organic phase was dried over Na2SO4 and evaporated to provide the title intermediate which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514997B2
Source datasetuspto-grants-2003_02
ORD IDord-922dbb5c2c104c169669214862f2bb92
Source noteuspto-grants-2003_02