Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | HCID 88672495 | HCID 88672495 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 13219901 | HCID 13219901 | 51.2% |
Reaction Steps
A mixture of 48 mg of (3S, 4R)-4-([2-(p-nitrobenzyloxycarbonylamino)ethylthio]carbonylmethyl)-3-[(R)-1-(p-nitrobenzyloxycarbonyloxy)ethyl]-1-[1-(p-nitrobenzyloxycarbonyl)-1-triisopropoxyphosphoranylidenemethyl]-2-azetidinone and 30 mg of hydroquinone in 5 ml of xylene was heated at 120° C. under a stream of a nitrogen gas for 13 hours. The xylene was then distilled off and the residue was subjected to chromatography using a Lobar column A eluted with a 2:1 by volume mixture of chloroform and ethyl acetate, to give crude crystals, which were recrystallized from a mixture of benzene and ethyl acetate, affording 19 mg (yield 51%) of colourless prisms, melting at 148°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05856556 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-411d238bfa2f41eb8cc114bc92e7566b |
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| Source note | uspto-grants-1999_01 |
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