HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653294Generated: October 28, 2026
Methylhydrazine → HCID 70390924, compound
https://huagongshe.com/reaction/653294
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | HCID 70390605 | HCID 70390605 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70390924 | HCID 70390924 | 87.6% |
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
| 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-c4f5b7db39344cc08f5331bf16b0be81 |
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| Source note | uspto-grants-1987_06 |
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