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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809388Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 59267897, compound

https://huagongshe.com/reaction/1809388

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantEthyl 2-(1-azetidinylsulfinyl)-2-methylpropanoateHCID 59267857—
SolventDichloromethaneHCID 6344—
ProductHCID 59267897HCID 59267897101.2%

Reaction Steps

To a solution of 4.62 g (21 mmol) of 2-(azetidine-1-sulfinyl)-2-methyl-propionic acid ethyl ester in DCM (100 mL) at room temperature are added 5.46 g (32 mmol) of meta-chloroperbenzoic acid. The reaction is stirred for 1 h before Ambersep 900-OH resin (2.9 g) is introduced. The suspension is shaken for 2 h and then filtered. The filtrate is concentrated under reduced pressure. The residue is dissolved in DCM (50 mL) and washed with a saturated aqueous NaHCO3 solution (50 mL). The organic layer is dried (Na2SO4) and filtered. The solvent is removed under reduced pressure to provide 5 g of 2-(azetidine-1-sulfonyl)-2-methyl-propionic acid ethyl ester as an orange oil, which is used in the next step without further purification. Yield 100%, ES-MS: m/z 236 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362039B2
Source datasetuspto-grants-2013_01
ORD IDord-9865885724f54d17b362a5710c02ade1
Source noteuspto-grants-2013_01