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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810171Generated: October 30, 2026

HCID 58107428, compound → HCID 58107440, compound

https://huagongshe.com/reaction/1810171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58107428HCID 58107428—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 58107440HCID 58107440—

Reaction Steps

2-Chloro-5-[hydroxy-(4-butoxy-phenyl)-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 10-50%) affording 74 mg of the title compound. 1H NMR (CDCl3) 0.95 (t, 3H, J=7.31 Hz), 1.50 (m, 2H), 1.80 (m, 2H), 4.05 (t, 2H, J=6.48 Hz), 5.15 (s, 2H), 6.95 (d, 2H, J=9.04 Hz), 7.65 (d, 1H, J=8.22), 7.80 (d, 2H, J=9.04 Hz), 7.90 (dd, 1 h, J=1.88, 7.91), 8.45 (d, 1H, J=1.88). MS (m/z): 368 (M+1). CHN Calc C, 55.51; H, 4.93; N, 3.81. Found C, 55.47; H, 4.84; N, 3.63.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362063B2
Source datasetuspto-grants-2013_01
ORD IDord-1b5695a6fc1c49979a3e37763e112a7f
Source noteuspto-grants-2013_01