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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335368Generated: October 26, 2026

Water → 2-(2-Hexyldecyl)thiophene

https://huagongshe.com/reaction/335368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThiopheneHCID 8030—
Reactant7-(Iodomethyl)pentadecaneHCID 58098323—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Hexyldecyl)thiopheneHCID 6750745777%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of thiophene (46.4 g, 551 mmol., 2.50 equiv.) and THF (300 mL) was cooled to −78° C. n-Butyllithium (2.5 M in hexanes, 212 mL, 528 mmol., 2.40 equiv.) was added over 1 hour. The mixture was stirred for an additional 30 minutes at −78° C. before a solution of 1-iodo-2-hexyldecane (90.0 g, 220 mmol., 1.00 equiv) in THF (200 mL) was added slowly over 1 hour. After stirring for 1 hour at −78° C., the reaction mixture was warmed to ambient temperature and stirred for 18 hours. Water (200 mL) was added and the organic material was extracted with Et2O (3×250 mL), washed with additional water, dried over Na2SO4, filtered, and concentrated in vacuo. The resulting brown residue was purified by silica gel column chromatography (hexanes) to give a pale yellow oil (52.03 g, 77% yield). 1H NMR (500 MHz, CDCl3) δ 7.12 (dd, J=5.2, 1.2 Hz, 1H), 6.92 (m, 1H), 6.76 (dd, J=3.4, 0.9 Hz, 1H), 2.76 (d, J=6.7, 2H), 1.62 (b, 1H), 1.33-1.21 (m, 24H), 0.91-0.87 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883958B2
Source datasetuspto-grants-2014_11
ORD IDord-24d8625866924b818ea5da32036bded2
Source noteuspto-grants-2014_11