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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827320Generated: October 30, 2026

Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 86596759, compound

https://huagongshe.com/reaction/1827320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(Dimethoxymethyl)-2,4-dimethoxybenzeneHCID 14287325—
ReactantHCID 22137749HCID 22137749—
SolventBenzeneHCID 241—
ProductHCID 86596759HCID 8659675974%

Reaction Steps

A hot solution of 6.6 g N-(2-nitrobenzenesulfenyl)-3-phenylisoserine in 100 ml of dry benzene is added with 0.5 g of pyridinium p-toluenesulfonate and 5.3 g of 2,4-dimethoxybenzaldehyde dimethylacetal. The solution is refluxed for 4 hours, then left to cool to room temperature. After that, 10 ml of a NaHCO3 saturated solution are added and the phases are separated. The aqueous phase is extracted with ethyl acetate and the combined organic phases are dried over Na2SO4 and evaporated under reduced pressure. The residual yellow oil is purified by chromatography (silica,hexane-ethyl acetate 5:1 with 2% triethylamine) to give the desired product in 74% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053222B2
Source datasetuspto-grants-2006_05
ORD IDord-46d723a0ac1c40b2a60a4de374268db4
Source noteuspto-grants-2006_05