HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507132Generated: November 2, 2026
Potassium tert-butoxide → (4aS,7aR)-Hexahydro-cyclopenta[d][1,3]oxazin-2-one
https://huagongshe.com/reaction/1507132
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | tert-butyl N-[(1R,2S)-2-(hydroxymethyl)cyclopentyl]carbamate | HCID 66545288 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4aS,7aR)-Hexahydro-cyclopenta[d][1,3]oxazin-2-one | HCID 117871704 | 91% |
Reaction Steps
To a solution of ((1R,2S)-2-hydroxymethyl-cyclopentyl)-carbamic acid tert-butyl ester (1.6 g, 7.43 mmol) in THF (40 ml) was added potassium tert-butoxide (3.34 g, 29.7 mmol, 4.0 equiv.) at room temperature. After stirring for 1 h at 60° C. the reaction was allowed to warm up to room temperature and after workup with Ethyl acetate/water, drying and concentration in vacuo, the crude material mixture was adsorbed on silica and chromatographed over a prepacked silica column (50 g, 50% to 100% EtOAc in Heptane gradient) to yield 950 mg (91%) of the title compound as a white solid, which was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221802B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-c3e7989562804a96ac19cb96d398473f |
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| Source note | uspto-grants-2015_12 |
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