HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682170Generated: October 30, 2026
Water → cis-3-hydroxy-4-phenylazetidin-2-one
https://huagongshe.com/reaction/1682170
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | cis-3-acetoxy-4-phenylazetidin-2-one | HCID 11009062 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | cis-3-hydroxy-4-phenylazetidin-2-one | HCID 10219588 | 97% |
Reaction Steps
To a solution of 200 mL of THF and 280 mL of 1M aqueous potassium hydroxide solution at 0° C. was added a solution of 4.59 g (22.4 mmol) of cis-3-acetoxy-4-phenylazetidin-2-one in 265 L of THF via a dropping tunnel over a 40 min period. The solution was stirred at 0° C. for 1 h and 100 mL of water and 100 mL of saturated sodium bicarbonate were added. The mixture was extracted with four 200 mL portions of ether acetate and the combined organic layers were dried over sodium sulfate and concentrated to give 3.54 g (97%) of racemic cis-3-hydroxy-4-phenylazetidin-2-one as white crystals, m.p. 147°-149° C. This material was resolved into its enantiomers by recrystallization of its 2-methoxy-2-(trifluoromethyl)phenylacetic ester from hexane/acetone followed by hydrolysis, [α]25Hg 177°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05175315 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-f5e4ab61c82a44f78f6da817b3b267fc |
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| Source note | uspto-grants-1992_12 |
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