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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542791Generated: October 31, 2026

2-Butanethiol → HCID 13850621, compound

https://huagongshe.com/reaction/542791

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ButanethiolHCID 10560—
ReactantThionyl ChlorideHCID 24386—
ReactantN-(2,2,2-trichloro-1-hydroxyethyl)nicotinamideHCID 246390—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(1,2,2,2-tetrachloroethyl)nicotinamideHCID 20207309—
SolventBenzeneHCID 241—
SolventTriethylamineHCID 8471—
ProductHCID 13850621HCID 1385062139.4%

Reaction Steps

150 ml of benzene was added to 5.0 g of N-(1-hydroxy-2,2,2-trichloroethyl)nicotinamide. 2.6 g of thionyl chloride was added dropwise to the mixture under stirring. Then, the mixture was heated under reflux (60° to 80° C.) for about 5 h to complete the production of N-(1,2,2,2-tetrachloroethyl)nicotinamide. The reaction liquid was cooled to 30° C. or below and 1.7 g of sec-butylmercaptan was added thereto. 3.7 g of triethylamine was added dropwise to the liquid mixture while it was kept at 5° C. The obtained mixture was stirred at room temperature for 3 h and then left to stand at room temperature overnight. The reaction liquid was poured in an aqueous sodium bicarbonate solution and a benzene layer thus separated was washed with a saturated aqueous common salt solution and water and then dried over anhydrous sodium sulfate. After concentration, the residue was recrystallized from a solvent mixture of n-hexane and ethyl acetate to obtain 2.5 g of N-(1-sec-butylthio-2,2,2-trichloroethyl)nicotinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659722
Source datasetuspto-grants-1987_04
ORD IDord-633544fb6d63477e8abcac332e0a8c67
Source noteuspto-grants-1987_04