HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858388Generated: November 1, 2026
Sulfuric Acid → (S)-2-Hydroxymethyl-azetidine-1-carboxylic acid benzyl ester
https://huagongshe.com/reaction/1858388
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (S)-Azetidin-2-ylmethanol | HCID 10855374 | — |
| Product | (S)-2-Hydroxymethyl-azetidine-1-carboxylic acid benzyl ester | HCID 10900173 | 96% |
Reaction Steps
Said solution of (S)-azetidine-2-methanol was adjusted to pH 10 by adding 10% sulfuric acid, sodium hydrogen carbonate (0.44 g, 5.29 mmol) was then added, and benzyloxycarbonyl chloride (0.88 g, 5.16 mmol) was added thereto at room temperature, followed by 14 hours of stirring. The solution was adjusted to pH 7 and extracted with ethyl acetate (50 mL ×2), the extract was washed with water (50 mL×1), dried over magnesium sulfate and filtered, and the filtrate was concentrated. The concentrate was subjected to column chromatography (Wakogel C-200) using toluene/ethyl acetate (1/1) as a mobile phase for separation/purification, to give (S)-N-benzyloxycarbonylazetidine-2-methanol (0.499 g, yield 96%) as a pale yellow oil. (S)-2-N-benzyloxycarbonyl-1,4-butanediol was obtained as a byproduct (0.032 g, yield 6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150535 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-830479ad1ad64e29b1fa3dfe11bd2f97 |
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| Source note | uspto-grants-2000_11 |
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