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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283113Generated: October 30, 2026

N-[(4-Methylphenyl)sulfonyl]-L-glutamic acid → HCID 12297768, compound

https://huagongshe.com/reaction/1283113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[(4-Methylphenyl)sulfonyl]-L-glutamic acidHCID 2063452—
Reactant4-Benzyl-2-toluene-p-sulphonyloxymethylmorpholineHCID 12297767—
SolventMethanolHCID 887—
ProductHCID 12297768HCID 1229776877.3%

Reaction Steps

To a solution of 4-benzyl-2-(toluene-p-sulphonyloxy)methylmorpholine (18.1 g.) in methanol (100 ml.) is added a solution of (+)-toluene-p-sulphonylglutamic acid (16.0 g.) in methanol (50 ml.) and the mixture is allowed to crystallise during 12 hours. The mixture is filtered and the residue (18.3 g.) is recrystallized from methanol (150 ml.) to obtain the (+)-toluene-p-sulphonylglutamic acid salt of (2S)-4-benzyl-2-(toluene-p-sulphonyloxy)methylmorpholine (14.0 g.), m.p. 184°C. This salt is stirred with a mixture of 2N sodium hydroxide and ether. The ether layer is separated, dried and the ether is distilled to leave optically pure (2S)-4-benzyl-2-(toluene-p-sulphonyloxy)methylmorpholine as an oil from which is prepared the hydrochloride, m.p. 150°C., [α]D25 + 19.4° (c,5 in methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03974158
Source datasetuspto-grants-1976_08
ORD IDord-f395e2d2ed8a42b6b9cd7c5f35c8a944
Source noteuspto-grants-1976_08