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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736018Generated: November 1, 2026

P-Anisidine → HCID 19434098, compound

https://huagongshe.com/reaction/1736018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantTriethylamineHCID 8471—
Reactant2-(3-Thienyl)-1,3-dioxolaneHCID 315630—
Reactant3-(1,3-dioxolan-2-yl)thiophene-2-sulfonyl ChlorideHCID 10538915—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19434098HCID 1943409875%

Reaction Steps

A solution of 3-(1,3-dioxolan-2-yl)-thiophene-2-sulfonyl chloride (11.16 g), prepared from thiophene-3-carboxaldehyde ethylene acetal as described in Example 6, Step A, in THF (100 mL) at 0° C. was combined with p-anisidine (7.87 g, 63.9 mmol) and triethylamine (4.04 g, 40 mmol). After stirring for 4 hr at ambient temperature, the mixture was evaporated to a residue which was extracted with ethyl acetate (2×150 mL). The combined extracts were dried (MgSO4) and evaporated to a residue which was purified by column chromatography (silica, 40% ethyl acetate/hexane) to give an oil (10.21 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538966
Source datasetuspto-grants-1996_07
ORD IDord-985edd1b453342fe82587fc02784107b
Source noteuspto-grants-1996_07