HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653302Generated: October 28, 2026
Propylene Oxide → cis-3-(1H-tetrazol-1-ylacetamido)-2-oxoazetidine-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/653302
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | (1H-Tetrazol-1-yl)acetyl chloride | HCID 13232854 | — |
| Reactant | cis-3-Amino-4-methoxycarbonyl-2-oxoazetidine | HCID 53988551 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | cis-3-(1H-tetrazol-1-ylacetamido)-2-oxoazetidine-4-carboxylic acid methyl ester | HCID 70390588 | 84% |
Reaction Steps
To a mixture of 288 mg of cis-3-amino-2-oxoazetidine-4-carboxylic acid methyl ester, 4 ml of propylene oxide and 3 ml of N,N-dimethylacetamide, which is stirred previously under ice-cooling, is added dropwise 400 mg of 1H-tetrazol-1-yl acetyl chloride, followed by stirring for 30 minutes. To the mixture is added 50 ml of ethyl ether, followed by stirring under cooling at -30° C., and then the upper layer is removed by decantation. The lower layer is subjected to the same procedure as above twice, followed by addition of 10 ml of acetone. The resultant solution is developed and purified by column-chromatography on silica-gel (40 g, 3×10 cm) using a mixture of acetone:methylene chloride (1:1) as eluent, followed by drying to give 403 mg (84%) of cis-3-(1H-tetrazol-1-ylacetamido)-2-oxoazetidine-4-carboxylic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04675397 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-b511baf3dc994a829728fab52d449494 |
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| Source note | uspto-grants-1987_06 |
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