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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809387Generated: October 31, 2026

Water → Ethyl 2-(1-azetidinylsulfinyl)-2-methylpropanoate

https://huagongshe.com/reaction/1809387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAzetidineHCID 10422—
ReactantChlorineHCID 24526—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2-(acetylthio)-2-methylpropanoateHCID 57937863—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(1-azetidinylsulfinyl)-2-methylpropanoateHCID 5926785780%

Reaction Steps

Chlorine gas is bubbled through a biphasic mixture of 5 g (26 mmol) of 2-acetylsulfanyl-2-methyl-propionic acid ethyl ester in DCM (50 mL) and water (50 mL) at 10° C. for 10 min. After this time, the organic phase is separated, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude sulfinyl chloride is re-dissolved in DCM (50 mL) and N,N-diisopropylethylamine (4.58 mL, 26 mmol) and azetidine (1.5 g, 26 mmol) are introduced. The reaction is stirred at room temperature for 1 h and then concentrated under reduced pressure. The residue is purified by column chromatography (silica, eluent heptanes, ethyl acetate) provides 4.62 g of 2-(azetidine-1-sulfinyl)-2-methyl-propionic acid ethyl ester. Yield: 80%, ES-MS: m/z 220 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362039B2
Source datasetuspto-grants-2013_01
ORD IDord-83c7b6ea2495482aa79b1a4c8ee9e695
Source noteuspto-grants-2013_01