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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-[(4-Methylphenyl)sulfonyl]-L-glutamic acid | HCID 2063452 | — |
| Reactant | 4-Benzyl-2-toluene-p-sulphonyloxymethylmorpholine | HCID 12297767 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12297768 | HCID 12297768 | 77.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03974158 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-f395e2d2ed8a42b6b9cd7c5f35c8a944 |
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| Source note | uspto-grants-1976_08 |
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