HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258426Generated: October 31, 2026
HCID 12804816, compound → HCID 12805476, compound
https://huagongshe.com/reaction/258426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 12804816 | HCID 12804816 | — |
| Reactant | 1011708-74-9 | HCID 23682957 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12805476 | HCID 12805476 | 74.1% |
Reaction Steps
To a solution of diphenylmethyl 2-[(3R,4R)-4-[(benzothiazol-2-yl)dithio]-3-phenoxyacetamido-2-oxo-azetidin-1-yl]-3-methyl-3-butenoate (XIIIa. 12.12 g, 0.0182 mole) in acetone (325 mL) and water (37 mL), silver nitrate (3.86 g, 0.0227 mole) was added all at once. A freshly prepared solution of sodium p-toluenesulfinate hydrate (4.05 g; 0.0227 mole) in acetone (255 mL) and water (37 mL) was added dropwise over 1 h, while the reaction mixture was protected from light. After an additional 1h period at room temperature, Celite (5 g) was added and the mixture was diluted with acetone (500 mL) and then was filtered. The filtrate was evaporated to a small volume, and the crude product was extracted into ether (3×250 mL). The ether phase was dried with magnesium sulfate and concentrated to afford a crude product. Flash chromatography (SiO2, eluting with 40% ethyl acetate in hexane) gave 9.05 g (73.5%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05266691 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-8d4c6a772b084f35beba24f23dfdd98d |
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| Source note | uspto-grants-1993_11 |
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