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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylene OxideHCID 6378—
ReactantDimethylacetamideHCID 31374—
Reactant(1H-Tetrazol-1-yl)acetyl chlorideHCID 13232854—
Reactantcis-3-Amino-4-methoxycarbonyl-2-oxoazetidineHCID 53988551—
SolventDiethyl EtherHCID 3283—
Productcis-3-(1H-tetrazol-1-ylacetamido)-2-oxoazetidine-4-carboxylic acid methyl esterHCID 7039058884%

Reaction Conditions

Temperature-30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04675397
Source datasetuspto-grants-1987_06
ORD IDord-b511baf3dc994a829728fab52d449494
Source noteuspto-grants-1987_06