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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192Generated: October 23, 2026

4-Methylmorpholine → (S)-N-(2-Phthalimido-1-oxohexyl)glycine, ethyl ester

https://huagongshe.com/en/reaction/1192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Reactant(S)-2-Phthalimido-6-hydroxyhexanoic acidHCID 11065730—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
Product(S)-N-(2-Phthalimido-1-oxohexyl)glycine, ethyl esterHCID 131719537—

Reaction Steps

A slurry of glycine, ethyl ester, hydrochloride salt (2.718 g, 19.5 mmol.) in dimethylformamide (36 ml.) was treated with 4-methyl morpholine (2.60 ml., 2.39 g., 23.6 mmol.) and stirred at room temperature for 5 minutes. The mixture was then treated with (S)-2-phthalimido-6-hydroxyhexanoic acid (4.50 g., 16.2 mmol.) and hydroxybenzotriazole (2.225 g., 16.5 mmol.), cooled to 0° C., and then treated with ethyl-3-(3-dimethylamino)propyl carbodiimide, hydrochloride salt (3.438 g., 17.9 mmol.). After stirring at 0° C. for 1 hour and at room temperature for 2 hours, the mixture was partitioned between ethyl acetate and 0.5N hydrochloric acid and subsequently extracted three times with ethyl acetate. The pooled ethyl acetate extracts were washed in succession with water, saturated sodium bicarbonate, and brine, then dried (sodium sulfate), filtered and stripped to give 5.77 g. of title product as a colorless oil. TLC (ethyl acetate) Rf =0.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723457
Source datasetuspto-grants-1998_03
ORD IDord-64ae065485524aae852fadf8328767e1
Source noteuspto-grants-1998_03