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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534341Generated: November 2, 2026

Triethylamine → HCID 15037082, compound

https://huagongshe.com/reaction/1534341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-(1-Aminotridecyl)-5-trimethylsilylfuranHCID 15037077—
SolventDichloromethaneHCID 6344—
ProductHCID 15037082HCID 15037082—

Reaction Steps

Methanesulfonyl chloride (37 μl, 0.48 mmol) was added to a solution of 3-(1-aminotridecyl)-5-trimethylsilylfuran (134.6 mg, 0.4 mmol) and triethylamine (67 μl, 0.48 mmol) in dichloromethane (2 ml) at 0°. Stirring continued overnight (14 hours) while the cooling both attained room temperature. The reaction mixture was quenched with water. Extraction (ethyl ether) and evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 10% ethyl ether/hexane. Fractions with Rf of about 0.07 on evaporation gave the title sulfonamide as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089485
Source datasetuspto-grants-1992_02
ORD IDord-7481f22f8a1b49d5ab74b1515c6c9c2d
Source noteuspto-grants-1992_02