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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021291Generated: October 30, 2026

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

https://huagongshe.com/reaction/1021291

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 1 M 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 numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-1a1dc289460e47c1866b9db05c90f0ce
Source noteuspto-grants-2014_05