HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903008Generated: October 31, 2026
HCID 20467711, compound → HCID 54399885, compound
https://huagongshe.com/reaction/1903008
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20467711 | HCID 20467711 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54399885 | HCID 54399885 | 83% |
Reaction Steps
4.5 g. (18.5 mmoles) of ethyl 1-(2-ethoxycarbonylethyl)-4-oxo-2-azetidine-carboxylate prepared according to Example 4 are dissolved in 20 ml. of dry ethanol, whereupon 1.4 g. (37 mmoles) of sodium tetrahydroborate(III) are added to the solution at 0° C., with stirring. The reaction mixture is stirred for an additional hour, and is then evaporated in vacuo, at room temperature. The residue is dissolved in 20 ml. of saturated aqueous hydrochloric acid solution and the pH of the solution is adjusted to 6.5 by addition of a 5% aqueous hydrochloric acid solution. The mixture is extracted with three 30-ml. portions of chloroform, dried with magnesium sulfate and filtered. The remaining solution is evaporated in vacuo. 3.1 g. (83%) of the named compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04435322 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-b4e24b8714294350ae242d70ecef6d27 |
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| Source note | uspto-grants-1984_03 |
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