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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343979Generated: October 30, 2026

Pyridine → HCID 54045408, compound

https://huagongshe.com/reaction/343979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 54222621HCID 54222621—
SolventChloroformHCID 6212—
ProductHCID 54045408HCID 5404540896.2%

Reaction Steps

To a solution of 1.05 g (6.7×10-3 mol) of 4-(3-thienyl)-butanol in 25 ml of dry, freshly distilled pyridine was added 0.85 g (1.1 equiv.) of methane-sulfonyl chloride at 25° C. The addition was gradual and carried out over a-several minute period. The reaction mixture was stirred for 6 hr at room temperature and quenched by pouring into a separtory funnel containing water-HCl and ether. The layers were separated and the aqueous layer was extracted once with 10% hydrochloric acid, followed by extraction with water and drying with Na2SO4Evaporation of the solvent afforded 1.51 g of a light brown oil (95% yield), tlc (CHCl3) showed a single spot. El. Anal. Calcd. for C9H14O3S2 : C, 46.13; H, 6.02; S, 27.36. Found: C, 45.92; H, 5.94; S, 27.15. Nmr (CDCl3 δ rel TMS) 2.0-1.5 brs, 4H; 2.67 brt, 2H; 2.97s, 3H; 4.22t, 2H; 7.07-6.80d, 2H; 7.37-7.13, 1H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05863981
Source datasetuspto-grants-1999_01
ORD IDord-b0523a27ffd64b8f9cc5c181146014c3
Source noteuspto-grants-1999_01