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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457340Generated: October 30, 2026

4-Methylmorpholine → HCID 15521370, compound

https://huagongshe.com/reaction/1457340

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl chloroformateHCID 10928—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
ReactantHCID 15521369HCID 15521369—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15521370HCID 15521370—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-[(4-methoxybenzenesulfonyl)methyl]-3-phenyl-propionic acid (1.05 g, 3.14 mmol) and 0.69 mL (6.3 mmol) of NMM in dry THF, under nitrogen, is cooled in an ice bath. Ethyl chloroformate (0.33 mL, 3.5 mmol) in 7 mL of THF is added dropwise over 5 minutes. The suspension is stirred at 0° C. for 10 minutes, after which a slurry of O-benzylhydroxylamine hydrochloride (0.64 g, 4 mmol) and NMM (0.44 mL, 4 mmol) in 7 mL of THF is introduced in several portions. The mixture is stirred for 10 minutes and stored at 10° C. overnight. The mixture is allowed to warm to room temperature for 0.5 hours, and is then partitioned between ethyl acetate and aqueous 10% HCl. The organic phase is washed with water, three portions of 1M sodium bicarbonate and brine. It is dried over anhydrous sodium sulfate, concentrated and chromatographed on silica gel, eluting with 40%-50% ethyl acetate in hexanes. This affords 1.26 g of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05847153
Source datasetuspto-grants-1998_12
ORD IDord-f7f04709b5ee46eaa70da1acb1709c9d
Source noteuspto-grants-1998_12