HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528726Generated: October 25, 2026
Iodine → tert-butyl (2S)-2-(hydroxymethyl)azetidine-1-carboxylate
https://huagongshe.com/reaction/528726
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | (2S)-1-((tert-butoxy)carbonyl)azetidine-2-carboxylic acid | HCID 2734495 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl (2S)-2-(hydroxymethyl)azetidine-1-carboxylate | HCID 10511797 | — |
Reaction Steps
To 699 mg (18.48 mmol) sodium borohydride in 20 mL dry THF under nitrogen, was added 1.15 g (5.74 mmol) (S)-azetidine-1,2-dicarboxylic acid 1-tert-butyl ester and the reaction was cooled to 0° C., 1.72 g (6.78 mmol) iodine in 10 mL dry THF was added dropwise over 30 minutes, the reaction mixture was allowed to warm to room temperature, and was heated under reflux for 19 hours. The mixture was cooled to room temperature and 25 mL MeOH was added dropwise over 15 minutes. After evaporation of the solvent, 30 mL KOH (1 M) was added and the mixture was stirred at room temperature for 2 hours. The aqueous phase was extracted with DCM (2×75 mL) and the combined organic layers were washed with saturated brine (3×50 mL), then dried over MgSO4. After filtration, the solvent was evaporated to give the desired product, which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346816B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-3361cd3c7f224f239212786508c241b6 |
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| Source note | uspto-grants-2016_05 |
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