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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256000Generated: October 25, 2026

1-Iodohexane → 1-Methoxy-3-(1-octynyl)benzene

https://huagongshe.com/reaction/256000

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodohexaneHCID 12527—
Reactant1-Ethynyl-3-methoxybenzeneHCID 640753—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-Methoxy-3-(1-octynyl)benzeneHCID 11264406—

Reaction Conditions

Temperature-70 °C

Reaction Steps

3-Methoxyphenylacetylene [5.00 g, 0.032M, prepared by the method of E. Negishi et al, J. Org. Chem. 45 2526-8, (1980)] was dissolved in dry tetrahydrofuran (15 ml), cooled to -70° C. under nitrogen, and n-butyl lithium, 1.6M in hexane, (24.40 ml, 0.038M), added dropwise. After stirring for 0.5 h, iodohexane (8.00 g, 0.038M), dissolved in dry tetrahydrofuran, (15 ml) was added dropwise. The rection was warmed slowly to room temperature, refluxed overnight, then cooled. The solution was then quenched with water, acidified with dilute hydrochloric acid and extracted with diethyl ether (twice). The organic phases were combined, washed with water and dried, (MgSO4). Evaporation in vacuo affored 7.71 g of product as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699995
Source datasetuspto-grants-1987_10
ORD IDord-b406641224384b73a1452fc6b9686c3f
Source noteuspto-grants-1987_10