HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703591Generated: October 29, 2026
Pyridine → allyl (4R)-4-[(2R,3S)-3-{(1R)-1-allyloxycarbonyloxyethyl}-4-oxoazetidin-2-yl]-2-diazo-3-oxopentanoate
https://huagongshe.com/reaction/703591
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Allyl chloroformate | HCID 18052 | — |
| Reactant | (3S,4R)-3-[(R)-1-hydroxyethyl]-4-[(R)-1-methyl-3-diazo-3-allyloxycarbonyl-2-oxopropyl]-2-azetidinone | HCID 54331596 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | allyl (4R)-4-[(2R,3S)-3-{(1R)-1-allyloxycarbonyloxyethyl}-4-oxoazetidin-2-yl]-2-diazo-3-oxopentanoate | HCID 57256977 | — |
Reaction Steps
To a solution of allyl (4R)-2-diazo-4-[(2R,3S)-3-{(1R)-1-hydroxyethyl}-4-oxoazetidin-2-yl]-3-oxopentanoate (14.6 g) in dichloromethane (100 ml) was added pyridine (6.05 ml) and allyl chloroformate (10.7 ml) at -78° C. The mixture was allowed to warm to ambient temperature and stirred for one day at the same temperature. The reaction mixture was poured into ethyl acetate (100 ml) and water (50 ml), washed in turn with water (50 ml) and brine (50 ml×2), and dried over magnesium sulfate. Evaporation of the solvent gave a residue, which was chromatographed on silica gel (500 ml) eluting with a mixture of hexane and ethyl acetate (1:1 V/V) to give allyl (4R)-4-[(2R,3S)-3-{(1R)-1-allyloxycarbonyloxyethyl}-4-oxoazetidin-2-yl]-2-diazo-3-oxopentanoate (10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983596 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-8729cfb8a5b949929ff3458ba5f39432 |
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| Source note | uspto-grants-1991_01 |
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