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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356832Generated: November 1, 2026

Hexane → HCID 18509434, compound

https://huagongshe.com/reaction/1356832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantHCID 12069881HCID 12069881—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18509434HCID 1850943457.4%

Reaction Steps

Methyl triphenylphosphonium bromide (1.97 g; 5.51 mmol) was suspended in tetrahydrofuran (15 ml). While the suspension was stirred under nitrogen atmosphere at room temperature, n-butyl lithium in n-hexane (1.68 M: 3.9 ml; 6.60 mmol) was added dropwise. After the reaction mixture turned deep red, the mixture was cooled in an ice bath, and Compound 1 (1.42 g; 4.59 mmol) in tetrohydrofuran (15 ml) was added dropwise thereto. After completion of the addition, the mixture was removed from the ice bath, and stirred for 30 minutes at room temperature. Reaction was stopped by pouring the mixture into ice/water, followed by extraction with diethyl ether (100 ml). The organic layer was washed with saturated aqueous sodium bicarbonate solution and then with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=10:1), to thereby yield 0.81 g of the target compound as yellow oily matter (yield: 57.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586633B1
Source datasetuspto-grants-2003_07
ORD IDord-29a0a920d33a4ceca85d759c256b58fa
Source noteuspto-grants-2003_07