Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508630Generated: October 30, 2026

1-Methylimidazole → HCID 131734116, compound

https://huagongshe.com/reaction/1508630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantEthyl AcetateHCID 8857—
Reactant2,4,5-Trichlorobenzenesulfonyl chlorideHCID 27575—
ReactantHCID 131734117HCID 131734117—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 131734116HCID 13173411681.5%

Reaction Steps

5.51 g of 2,4,5-trichlorobenzenesulfonyl chloride and 2.14 mL of 1-methylimidazole were added to a solution of 6.65 g of (2R,3S)-2-hydroxy-5-(methoxyimino)pentane-1,3-diyl dibenzoate in 67 mL of acetonitrile at room temperature, and the obtained mixture was then stirred at room temperature for 2 hours. Thereafter, ethyl acetate and water were added to the reaction mixture. The organic layer was fractionated, and was then dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure. 20 mL of ethyl acetate and 30 mL of hexane were added to the obtained residue, and a solid was then removed by filtration. After that, the solvent was distilled away under reduced pressure, so as to obtain 8.97 g of (2R,3S)-5-(methoxyimino)-2-(((2,4,5-trichlorophenyl)sulfonyl)oxy)pentane-1,3-diyl dibenzoate in the form of a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221865B2
Source datasetuspto-grants-2015_12
ORD IDord-2852106c0a0b4d938bf25aa3595042f8
Source noteuspto-grants-2015_12