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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489428Generated: October 30, 2026

Triethylamine → HCID 10578947, compound

https://huagongshe.com/reaction/1489428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 10814962HCID 10814962—
SolventEthyl AcetateHCID 8857—
ProductHCID 10578947HCID 10578947104.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-[(1R,2S)-2-(2,4-Difluorophenyl)-2,3-dihydroxy-1-methylpropyl]-4-[4-(2,2,3,3-tetrafluoropropoxy)phenyl]-3(2H,4H)-1,2,4-triazolone (8.26 g) was dissolved in 100 ml of ethyl acetate, to which 2.89 g of methanesulfonyl chloride and 2.54 g of triethylamine were added dropwise with ice cooling. After stirring at 0° C. for 30 minutes, the solution was washed with water (20 ml×2) and 20 ml of an aqueous solution of sodium chloride successively. The organic layer was dried over magnesium sulfate. The solvent was distilled off under reduced pressure to give 10 g of 2-[(1R,2S)-2-(2,4-difluorophenyl)-2-hydroxy-3-methanesulfonyloxy-1-methylpropyl]-4-[4-(2,2,3,3-tetrafluoropropoxy)phenyl]-3(2H,4H)-1,2,4-triazolone as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677464
Source datasetuspto-grants-1997_10
ORD IDord-cf08fd39866a4aafac18270d1c8486bd
Source noteuspto-grants-1997_10