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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728330Generated: November 1, 2026

Hexane → HCID 19002942, compound

https://huagongshe.com/reaction/1728330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19002960HCID 19002960—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19002942HCID 1900294292.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In 5 ml of dry tetrahydrofuran is dissolved 300 mg of 1-benzyloxymethyl-4-methyl-5-phenylthioimidazole (I-3) (1 mmol) obtained in Example 3, and the resulting solution is chilled at -78° C. To the solution is added dropwise 1.64M solution of n-butyl lithium in 0.71 ml of hexane (1.16 mmol) and the mixture allowed to stand for 10 minutes, when 185 mg of bromine (1.16 mmol) is added thereto. Fifteen minutes later, the mixture is poured onto ice water. The mixture is neutralized with sodium bicarbonate and extracted with ethyl ether. The extract is washed with water, dried over sodium sulfate, filtered and the filtrate is concentrated. The crude product is chromatographed on a column of silica gel, eluting with ethyl acetate/n-hexane (1:2) to give 360 mg of the product (I-20; mp. 55° C.). Yield, 96%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05326780
Source datasetuspto-grants-1994_07
ORD IDord-961afa9678d14e02b33187699996f1c9
Source noteuspto-grants-1994_07