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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 2-(acetylthio)-2-methylpropanoate | HCID 57937863 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(1-azetidinylsulfinyl)-2-methylpropanoate | HCID 59267857 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08362039B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-83c7b6ea2495482aa79b1a4c8ee9e695 |
|---|
| Source note | uspto-grants-2013_01 |
|---|