HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342289Generated: October 30, 2026
Sodium Chloride → HCID 86753533, compound
https://huagongshe.com/reaction/342289
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 13471478 | HCID 13471478 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86753533 | HCID 86753533 | 63% |
Reaction Steps
To a solution of 448 mg of (3S, 4S)-3-[(R)-1-(p-nitrobenzyloxycarbonyloxy)ethyl]-4-[(phenylthio)ethynyl]-2-azetidinone in 5 ml of anhydrous methylene chloride was added, under an atmosphere of nitrogen gas, 0.4 ml of trifluoroacetic acid, with stirring and ice-cooling. Stirring was continued for 30 minutes under ice-cooling and for a further 1.5 hours at room temperature. The reaction mixture was then poured into a mixture of 1.0 g of sodium bicarbonate, 10 ml of water and 20 ml of ethyl acetate. The mixture was saturated with sodium chloride and the organic layer was separated. The aqueous layer was extracted twice with ethyl acetate. The organic layer and the ethyl acetate extracts were combined, and the combined solution was washed successively with an aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulphate. The solvent was distilled off under reduced pressure and the residue was subjected to column chromatography through silica gel, eluted with a 1:1 by volume mixture of cyclohexane and ethyl acetate, to afford 95.0 mg (yield 63.0%) of the title thioester compound, as a viscous oil.
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-c590f632128245078f67bde4c7ececdc |
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| Source note | uspto-grants-1999_01 |
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