HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900221Generated: October 30, 2026
Water → cis-3-hydroxy-4-phenylazetidin-2-one
https://huagongshe.com/reaction/1900221
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 mixture of 200 mL of THF and 280 mL of 1 M 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 ml of THF via a dropping funnel 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 ethyl 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° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574156 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-ea35e5b37be04ff3aed7314886bf4e9f |
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| Source note | uspto-grants-1996_11 |
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