Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171691Generated: October 31, 2026

1,2-Dichloroethane → {3-[4-(Ethylsulfonyl)piperazin-1-yl]-2-fluorophenyl}methanol

https://huagongshe.com/reaction/2171691

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantChloroformHCID 6212—
ReactantEthanesulfonyl chlorideHCID 11667—
Reactant1-[3-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-2-fluorophenyl]piperazineHCID 86686202—
SolventWaterHCID 962—
Product{3-[4-(Ethylsulfonyl)piperazin-1-yl]-2-fluorophenyl}methanolHCID 6831025395%

Reaction Steps

1-[3-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-2-fluorophenyl]piperazine (140 mg) was mixed with DCE (4 ml), and ethanesulfonyl chloride (122 mg) and TEA (145 mg) were added thereto, followed by stirring at room temperature for 2 hours. CHCl3 and water were added to the reaction mixture, and the organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was mixed with THF (4 ml), and a 1M TBAF/THF solution (0.9 ml) was added thereto, followed by stirring at room temperature for 2 hours. EtOAc and water were added to the reaction mixture, and the organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (EtOAc/hexane) to obtain {3-[4-(ethylsulfonyl)piperazin-1-yl]-2-fluorophenyl}methanol (123.9 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051283B2
Source datasetuspto-grants-2015_06
ORD IDord-397e2b1ab52a4fd8ab9ae4adca70f7ba
Source noteuspto-grants-2015_06