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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632367Generated: October 30, 2026

Hexane → N-(2,2-Dimethyl-1-(thiazol-2-yl)propyl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/632367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantThiazoleHCID 9256—
Reactant(NE)-N-(2,2-dimethylpropylidene)-2-methylpropane-2-sulfinamideHCID 11506602—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductN-(2,2-Dimethyl-1-(thiazol-2-yl)propyl)-2-methylpropane-2-sulfinamideHCID 7108781492%

Reaction Conditions

Temperature-75 °C

Reaction Steps

To a solution of thiazole (247 mg, 206 μl, 2.91 mmol) in 10 mL dry THF under argon at −73° C. was slowly added a 1.6M solution of BuLi in hexane (1.82 ml, 2.91 mmol). The resulting reaction mixture was stirred at −75° C. for 30 min and a solution of (E)-N-(2,2-dimethylpropylidene)-2-methylpropane-2-sulfinamide (Example 306a) (500 mg, 2.64 mmol) in 5 mL dry THF was added. The reaction mixture was stirred at −75° C. for 30 min, then cooling bath was removed and reaction stirred at r.t for 1 h. The reaction was quenched by the addition of few drops of water, the reaction mixture poured into ethyl acetate, and the solution was then extracted with aqueous NaHCO3 1M. The organic phase was collected, dried over Na2SO4 and evaporated down to dryness to give the title compound (666 mg, 92%) as crude dark orange oil. The crude was used without any further purification, MS (EI): m/e=275.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321727B2
Source datasetuspto-grants-2016_04
ORD IDord-091db97f0b244cc18b1bed33c4f72f2f
Source noteuspto-grants-2016_04