Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873649Generated: October 30, 2026

HCID 58107396, compound → HCID 44235743, compound

https://huagongshe.com/reaction/873649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58107396HCID 58107396—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 44235743HCID 44235743—

Reaction Steps

2-Chloro-5-[(4-pentyloxy-phenyl)-hydroxy-methyl]-benzenesulfonamide is dissolved in acetone (10 mL), and treated with a solution of Jones reagent (3 M in water, 0.91 mmol). The reaction is allowed to stir for 30 minutes. The reaction is diluted with water and extracted with dichloromethane. The organic phase is separated and concentrated in vacuo. The residue is purified by silica gel chromatography (gradient of ethyl acetate in hexanes 25-75%) followed by recrystallization from ether affording 15 mg of the title compound. 1H NMR (DMSO) 0.90 (t, 3H, J=6.79 Hz), 1.31-1.46 (m, 4H), 1.70-1.79 (m, 2H), 4.09 (t, 2H, J=6.49 Hz), 7.10 (d, 2H, J=9.04 Hz), 7.75-7.90 (m, 4H), 8.24 (d, 1H, J=1.89). MS (m/z): 382 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975439B2
Source datasetuspto-grants-2015_03
ORD IDord-d7a3b01b2abb4df5b5db97eb7d4d58b8
Source noteuspto-grants-2015_03