HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809388Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 59267897, compound
https://huagongshe.com/reaction/1809388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Ethyl 2-(1-azetidinylsulfinyl)-2-methylpropanoate | HCID 59267857 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59267897 | HCID 59267897 | 101.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362039B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-9865885724f54d17b362a5710c02ade1 |
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| Source note | uspto-grants-2013_01 |
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