HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615858Generated: November 3, 2026
HCID 86739940, compound → HCID 86739941, compound
https://huagongshe.com/reaction/615858
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86739940 | HCID 86739940 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86739941 | HCID 86739941 | 79.7% |
Reaction Steps
A solution of (±)-(cis)-[(3-azido-1-(4-methoxyphenyl)-2-oxo-4-azetidinyl)methoxy]acetic acid, methyl ester (2.054 g, 6.44 mmole) in acetonitrile (40 ml) was cooled to -5° C. A solution of ceric ammonium nitrate (10.62 g, 19.32 mmole) in water (30 ml) was added rapidly over ca. forty-five seconds. The reaction was warmed to +10° C. over fifteen minutes, diluted with water (100 ml), and extracted with ethyl acetate (two 80 ml portions). Sodium chloride was added to the aqueous layer which was again extracted with ethyl acetate (ca. 150 ml). The organic extracts were washed with saturated potassium bicarbonate, saturated sodium sulfite solution, brine, and dried (sodium sulfate). Filtration followed by solvent removal yielded 1.56 g of crude product which was chromatographed on silica gel (55 g, 230-400 mesh). Elution with 70% ethyl acetate-hexane yielded 1.1 g of the title compound as a heavy oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04501697 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-4d3d588d0a6341ce93f6bb42506f32b1 |
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| Source note | uspto-grants-1985_02 |
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