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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935591Generated: October 30, 2026

Ethanethiol → HCID 136401066, compound

https://huagongshe.com/reaction/1935591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 69545726HCID 69545726—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 136401066HCID 136401066—

Reaction Steps

Dimethylation was performed using Method 2 described for Step C in Scheme I. To a solution of the isoxazole obtained from step 6 (1.0 equiv.) in dichloroethane was added aluminum chloride (5.0 equiv.) and ethane thiol (5.0 equiv.). The resultant mixture was stirred for 40 min at room temperature and quenched with THF, 20% HCl and water. A precipitate was formed and this was collected by filtration. After drying the product the material was taken up in methanol, treated with activated charcoal, filtered through sodium sulfate and concentrated in vacuo. Purification with flash chromatography followed by addition of HCl aq. and lyophilization, then afforded the product 4-[5-(4-hydroxyphenyl)-4-[4-(2-piperidylethoxy)phenyl]isoxazol-3-yl]phenol as hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387920B2
Source datasetuspto-grants-2002_05
ORD IDord-5b10030b90274c49a1a0bbe9f70a26b5
Source noteuspto-grants-2002_05