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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366559Generated: November 2, 2026

Methyl chloroglyoxylate → methyl oxo((phenylmethyl){[(3R)-4-(phenylmethyl)-3-morpholinyl]methyl}amino)acetate

https://huagongshe.com/reaction/1366559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroglyoxylateHCID 79846—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-phenyl-N-{[(3R)-4-(phenylmethyl)-3-morpholinyl]methyl}methanamineHCID 66936439—
SolventTetrahydrofuranHCID 8028—
Productmethyl oxo((phenylmethyl){[(3R)-4-(phenylmethyl)-3-morpholinyl]methyl}amino)acetateHCID 66936387107.5%

Reaction Steps

To a solution of 1-phenyl-N-{[(3R)-4-(phenylmethyl)-3-morpholinyl]methyl}methanamine (3.3777 g, 11.40 mmol) in THF (114 mL) was added N,N-diisopropylethylamine (3 mL, 17.22 mmol). To the solution was added methyl chloro(oxo)acetate (1.15 mL, 12.50 mmol) dropwise via syringe, and the mixture was stirred for 3 h. The solvent was removed in vacuo, and the residue was dissolved in EtOAc (200 mL) and washed with sat. aq. NaHCO3 followed by water. The organic phase was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to afford crude methyl oxo((phenylmethyl){[(3R)-4-(phenylmethyl)-3-morpholinyl]methyl}amino)acetate (4.6881 g, >100% crude yield) as a yellow oil. LCMS: (M+H)+: 383.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-86da69760ace47718f44a18aa848e88c
Source noteuspto-grants-2011_02