HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528756Generated: October 29, 2026
Dimethyl Sulfoxide → Tert-butyl 3-formylazetidine-1-carboxylate
https://huagongshe.com/reaction/528756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | tert-Butyl 3-(hydroxymethyl)azetidine-1-carboxylate | HCID 10583745 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 3-formylazetidine-1-carboxylate | HCID 10726182 | — |
Reaction Steps
To 40 mL dry DCM was added 2.19 mL (30.8 mmol) DMSO. The solution was cooled to −78° C. under nitrogen and 1.95 mL (23.1 mmol) oxalyl chloride was added dropwise. A solution of 2.88 g (15.4 mmol) 3-hydroxymethyl-azetidine-1-carboxylic acid tert-butyl ester in 20 mL dry DCM was added quickly via syringe followed by 10.5 mL (77 mmol) triethylamine. The mixture was allowed to warm to room temperature and then quenched by extraction with 1 M HCl (2×50 mL). The organic layer was dried over Na2SO4, filtered and evaporated to give the product which was used in 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-5034c67141314341a4cf83667fb31a1d |
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| Source note | uspto-grants-2016_05 |
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