HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653287Generated: October 29, 2026
Sodium borohydride → HCID 70390815, compound
https://huagongshe.com/reaction/653287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70390633 | HCID 70390633 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70390815 | HCID 70390815 | 91.1% |
Reaction Steps
Under ice-cooling and stirring, 12 ml of an aqueous solution containing 570 mg of sodium borohydride is added to a solution of 2.06 g of cis-1-(2,4-dimethoxybenzyl)-3-phenylacetamido-2-oxoazetidine-4-carboxylic acid methyl ester in 24 ml of tetrahydrofuran. The reaction mixture is stirred for 30 minutes under ice-cooling and then for 1.5 hours at room termperature. The tetrahydrofuran is distilled off in vacuo and an aqueous sodium chloride solution and ethyl acetate are added to the residue. The resulting ethyl acetate layer is separated and washed successively with an aqueous sodium hydrogen carbonate and an aqueous sodium chloride. It is then dried over magnesium sulfate and the solvent is distilled off in vacuo. Ether is added to the residue and the precipitated crystals are collected by filtration to give 1.75 g (91%) of cis-1-(2,4-dimethoxybenzyl)-4-hydroxymethyl-3-phenylacetamido-2-oxoazetidine, m.p. 152°-154° C.
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-1437efa90e1f4006a7725ac54b5938ad |
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| Source note | uspto-grants-1987_06 |
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