HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271493Generated: November 2, 2026
Hydrochloric Acid → tert-Butyl 3-(hydroxymethyl)azetidine-1-carboxylate
https://huagongshe.com/reaction/2271493
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Boc-Azetidine-3-carboxylic acid | HCID 2755981 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 3-(hydroxymethyl)azetidine-1-carboxylate | HCID 10583745 | — |
Reaction Steps
Borane dimethyl sulfide complex (4.5 mL, 15.0 mmol) was slowly added to 1-(tertiary butoxycarbonyl)azetidine-3-carboxylic acid (1.0 g, 5.0 mmol) dissolved in a distilled tetrahydrofuran solution (20 mL) at 0° C., and the mixture was stirred at the same temperature for 4 hours. Thereafter, 1N HCl aqueous solution (70 mL) was slowly added at 0° C., and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was extracted with ethyl acetate (3*30 mL), and the organic layer was washed with a saturated sodium chloride solution and distilled water once, respectively and dried over anhydrous magnesium sulfate. The solvent was removed by reduced pressure evaporation to obtain the desired compound tertiary butyl 3-(hydroxymethyl)azetidine-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120771B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-a08b0a51f8ba4e3c95fb4780f37a7b44 |
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| Source note | uspto-grants-2015_09 |
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