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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | 1-[3-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-2-fluorophenyl]piperazine | HCID 86686202 | — |
| Solvent | Water | HCID 962 | — |
| Product | {3-[4-(Ethylsulfonyl)piperazin-1-yl]-2-fluorophenyl}methanol | HCID 68310253 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051283B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-397e2b1ab52a4fd8ab9ae4adca70f7ba |
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| Source note | uspto-grants-2015_06 |
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