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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653294Generated: October 28, 2026

Methylhydrazine → HCID 70390924, compound

https://huagongshe.com/reaction/653294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantHCID 70390605HCID 70390605—
SolventDichloromethaneHCID 6344—
ProductHCID 70390924HCID 7039092487.6%

Reaction Steps

To a solution of 19 g of cis-1-(2,4-dimethoxybenzyl)-3-phthalimido-2-oxoazetidine-4-carboxylic acid n-butyl ester in 190 ml of methylene chloride is added 3.7 g of methyl hydrazine. The mixture is stirred overnight at room temperature. The reaction mixture is subjected to filtration, and the filtrate is concentrated under reduced pressure. To the residue is added ethyl acetate, and the insolubles are removed by filtration. The filtrate is subjected to extraction twice, with 100 ml each of 1N--HCl. The extracts are neutralized with sodium hydrogen carbonate, and extracted with ethyl acetate. The extract is washed with an aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, followed by evaporation of the solvent under reduced pressure to yield 12 g (87.5%) of cis-3-amino-1-(2,4-dimethoxybenzyl)-2-oxoazetidine-4-carboxylic acid n-butyl ester as oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04675397
Source datasetuspto-grants-1987_06
ORD IDord-c4f5b7db39344cc08f5331bf16b0be81
Source noteuspto-grants-1987_06