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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515448Generated: November 4, 2026

HCID 58107396, compound → HCID 44235743, compound

https://huagongshe.com/reaction/1515448

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) δ 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 numberUS08222424B2
Source datasetuspto-grants-2012_07
ORD IDord-2c4aed7987bf46dd887b93d9f99c6d15
Source noteuspto-grants-2012_07