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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202241Generated: November 3, 2026

Methanol → CTK3C8796

https://huagongshe.com/reaction/2202241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant(S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonateHCID 2724793—
ReactantSodium methanolate methanolHCID 23694274—
SolventAcetic AcidHCID 176—
ProductCTK3C8796HCID 1088793953%

Reaction Steps

28% Sodium methoxide/MeOH solution (74.0 g, 383.35 mmol) was added to a mixture of (S)-(5-oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate (51.81 g, 191.67 mmol) and dehydrated MeOH (280 mL) at room temperature, and the mixture was stirred at room temperature for 1.5 hr. The reaction mixture was cooled under ice-cooling, and the mixture was neutralized with acetic acid (about 15 mL). The reaction mixture was concentrated to about half-volume under reduced pressure, and ice water (350 mL) was added thereto. Then, the mixture was extracted with a mixed solvent of ethyl acetate/diethyl ether (3:1) (×3). The organic layer was washed successively with aqueous sodium hydrogencarbonate solution, water and brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to give crude methyl (S)-3-(oxiran-2-yl)propanoate (13.12 g, 101 mmol, 53%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365520B2
Source datasetuspto-grants-2016_06
ORD IDord-95ed873ca1ea4e34a1a32e282c31d6cd
Source noteuspto-grants-2016_06