HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050383Generated: November 2, 2026
Lactic Acid → cis-4-Oxo-3-phenoxyacetylamino-2-p-toluenesulfonyloxymethylazetidine
https://huagongshe.com/reaction/2050383
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lactic Acid | HCID 612 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 70579374 | HCID 70579374 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | cis-4-Oxo-3-phenoxyacetylamino-2-p-toluenesulfonyloxymethylazetidine | HCID 86734329 | — |
Reaction Steps
To a solution of 4.30 g (0.022 mole) of 98% p-toluenesulfonyl chloride in 24 ml of anhydrous pyridine at 0° (ice bath) was added 2.64 g (0.011 mole) of cis-2-hydroxymethyl-4-oxo-3-phenoxyacetylaminoazetidine in one portion. The solution was stirred at 0° for 3 hours then was stored at -25° overnight. After warming to 0°, 1.0 ml of 85% lactic acid was added and stirring was continued for 1 hour. The reaction mixture was poured into ethyl acetate and extracted successively with water, dilute aqueous hydrochloric acid, aqueous sodium bicarbonate and brine and was dried (MgSO4). Filtration followed by removal of the solvent in vacuo resulted in a yellow solid. Clarification of a hot solution of this material in ethyl acetate (375 ml), followed by the addition of hexane (200 ml) and recrystallization afforded cis-4-oxo-3-phenoxyacetylamino-2-p-toluenesulfonyloxymethylazetidine; tlc: ethyl acetate, silica gel GF, Rf=0.47; mp 136° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04200572 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-610353e665a1442190ff2f8ae998d3f0 |
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| Source note | uspto-grants-1980_04 |
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