HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921653Generated: October 30, 2026
3-Hydroxyazetidine hydrochloride → HCID 86708505, compound
https://huagongshe.com/reaction/921653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxyazetidine hydrochloride | HCID 2759290 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86708505 | HCID 86708505 | — |
Reaction Steps
A mixture of oxetan-3-one (0.5 g, 6.94 mmol), azetidin-3-ol hydrochloride (1.140 g, 10.41 mmol) and 4 A molecular sieves (1.5 g) in dichloromethane (10 mL) was stirred at room temperature for 4 h. Sodium triacetoxyborohydride (2.94 g, 13.88 mmol) was added and the reaction mixture was stirred at room temperature overnight. The precipitate was filtered through a pad of celite and the filtrate was diluted with ethyl acetate (more precipitate appeared) and filtered again. The filtrate was concentrated in vacuo and the crude product was purified by flash chromatography on silica gel using an automated ISCO system (80 g column, eluting with 3-10% 2N ammonia in methanol/dichloromethane). 1-(oxetan-3-yl)azetidin-3-ol was obtained as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273057B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-43f4b08c5a0149f99af063e7861ee964 |
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| Source note | uspto-grants-2016_03 |
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