HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482846Generated: October 30, 2026
Hydrochloric Acid → HCID 20559124, compound
https://huagongshe.com/reaction/482846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20243661 | HCID 20243661 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20559124 | HCID 20559124 | 41% |
Reaction Steps
A mixture of methyl 2-(3-azido-4-formyl-2-oxo-1-azetidinyl)-2-phenylacetate (2.30 g.), sodium borohydride (310 mg), ethanol (40 ml.) and water (5 ml.) was stirred at -10° to 0° C. for an hour. The reaction mixture was adjusted to pH 4 to 5 with 10% hydrochloric acid at the same temperature, whereafter the ethanol was removed by distillation from the solution to give an aqueous residue, to which sodium chloride was added. The resultant solution was extracted twice with chloroform and the extract was washed with an aqueous sodium chloride. After drying the solution over magnesium sulfate, the solution was evaporated to dryness under reduced pressure to give a residue(2.02 g.), which was subjected to column chromatography on alumina(20 g.). Elution was carried out with chloroform and the fractions containing a desired compound were collected. The solvent was removed by distillation under reduced pressure to give methyl 2-(3-azido-4-hydroxymethyl-2-oxo-1-azetidinyl)-2-phenylacetate(0.95 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04576753 |
|---|
| Source dataset | uspto-grants-1986_03 |
|---|
| ORD ID | ord-f7aa1facfd654a278fc05447ef67fc42 |
|---|
| Source note | uspto-grants-1986_03 |
|---|