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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106896Generated: October 31, 2026

1-Hexanol → 3-(Hexyloxy)thiophene

https://huagongshe.com/reaction/2106896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HexanolHCID 8103—
Reactant3-MethoxythiopheneHCID 140249—
ReactantSodium BisulfateHCID 516919—
SolventTolueneHCID 1140—
Product3-(Hexyloxy)thiopheneHCID 11041417—

Reaction Conditions

Temperature125 °C

Reaction Steps

20 cm3 of 3-methoxythiophene (0.2 mol) and 50 cm3 of 1-hexanol were dissolved in 30 cm3 of toluene, and 1 g of NaHSO4 (0.01 mol) was added. The mixture was heated to 125° C. and stirred, and about 10 cm3 of a mixture of methanol and toluene were distilled off through a Vigreux column at a head temperature of 63° to 64° C., which took about 3 hours. The mixture was then washed three times with 50 cm3 of saturated NaHCO3 solution until neutral, dried over MgSO4 and fractionated in vacuo. After the toluene had been distilled off together with excess haxanol, 34 g of 3-n-hexyloxythiophene distilled over at 70° C. and 0.13 mbar, which corresponds to 92% of the theoretical yield. 97% pure by GC; 1H-NMR and mass spectrum confirm the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931568
Source datasetuspto-grants-1990_06
ORD IDord-6a040e908a4442d8a5cfd1d4e676defb
Source noteuspto-grants-1990_06