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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactanttert-Butyl 3-(hydroxymethyl)azetidine-1-carboxylateHCID 10583745—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 3-formylazetidine-1-carboxylateHCID 10726182—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346816B2
Source datasetuspto-grants-2016_05
ORD IDord-5034c67141314341a4cf83667fb31a1d
Source noteuspto-grants-2016_05