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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654227Generated: November 3, 2026

Methyl butyrate → HCID 14978400, compound

https://huagongshe.com/reaction/1654227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl butyrateHCID 12180—
ReactantMethyl 3-mercaptopropionateHCID 18050—
Reactant1H-1,2,4-Triazole, 1-[[(2S,3S)-2-(2,4-difluorophenyl)-3-methyloxiranyl]methyl]-HCID 11345723—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
ProductHCID 14978400HCID 14978400—

Reaction Steps

In methanol (25 ml) were dissolved (2S,3S)-2-(2,4-difluorophenyl)-3-methyl-2-[(1H-1,2,4-triazol-1-yl)methyl]oxirane (1.0 g), methyl 3-mercaptopropionate (3.5 ml) and 28% sodium methoxide-methanol (3.07 g) and the solution was refluxed in an oil bath. After 2 and after 3 hours, methyl 3-methylpropionate (1.75 ml) and 28% sodium methoxide-methanol (1.5 g) were added at each time. The oil bath was removed after heating for 4 hours and the reaction mixture was neutralized with cold 1N hydrochloric acid (32 ml) and extracted with dichloromethane (200 ml). The extract was washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: hexane-ethyl acetate=1:3). The desired fraction was concentrated and the resulting crystals were recrystallized from ethyl acetate-hexane to give (2S,3R)-2-(2,4-difluorophenyl)-3-mercapto-1-(1 H-1,2,4-triazol-1-yl)-2-butanol (compound 117, 472 mg) as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405861
Source datasetuspto-grants-1995_04
ORD IDord-9d6e9f68e2a54cd98ac56c5e3b4e81c4
Source noteuspto-grants-1995_04