HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506841Generated: October 31, 2026
Benzyl chloroformate → Benzyl 3-hydroxyazetidine-1-carboxylate
https://huagongshe.com/reaction/1506841
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Hydroxyazetidine | HCID 1514290 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 3-hydroxyazetidine-1-carboxylate | HCID 10081755 | 69.8% |
Reaction Steps
A solution of azetidin-3-ol (14.7 g) dissolved in THF (170 mL) and water (85 mL) was treated with potassium carbonate (37.1 g) under nitrogen. The mixture was stirred at RT for 30 minutes before cooling to 0° C. and adding benzyl carbonochloridate (20.0 mL) dropwise over 30 minutes at 0° C. The resulting mixture was stirred at 20° C. for 60 hours. The reaction mixture was diluted with water (150 mL), and extracted with ethyl acetate (200 mL). The organic was dried over magnesium sulfate, filtered and evaporated to afford crude product as a colourless oil. The crude product was purified by flash silica chromatography, elution 50% ethyl acetate in isohexane to 100% ethyl acetate. Pure fractions were evaporated to dryness to afford the sub-title product (19.40 g, 69.8%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221782B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-9d49e11a7df84b8caa27e777cf3c277e |
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| Source note | uspto-grants-2015_12 |
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