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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575501Generated: October 30, 2026

Hexane → HCID 71245442, compound

https://huagongshe.com/reaction/575501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDodecanoyl chlorideHCID 8166—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4,9-Dimethoxynaphtho[1,2-b:5,6-b']dithiopheneHCID 71245676—
SolventDichloromethaneHCID 6344—
ProductHCID 71245442HCID 7124544254%

Reaction Steps

4,9-Dimethoxynaphtho[1,2-b:5,6-b′]dithiophene (0.90 g, 3.0 mmol) was solubilized in anhydrous dichloromethane (20 mL). Dodecanoyl chloride (0.765 g, 3.5 mmol) was then added and stirring was continued for 10 minutes at this temperature. Aluminum trichloride (0.465 g, 3.5 mmol) was then added in 3 portions. The mixture was stirred overnight at room temperature. The mixture was cooled in ice water and extracted with chloroform (200 mL) and washed with water (100 mL) and brine (50 mL). After the solvent was removed, the residual was purified using a silica column with dichloromethane:hexane (1/3) to give compound 1-(4,9-dimethoxynaphtho[1,2-b:5,6-b′]dithiophen-2-yl)dodecan-1-one as a pale yellow solid (0.78 g, ˜54% yield). 1H NMR (500 MHz, CDCl3): δ 8.72 (s, 1H), 7.69 (d, J=5.5 Hz, 1H), 7.50 (m, 2H), 7.42 (s, 1H), 4.24 (s, 3H), 4.22 (s, 3H) 3.07. (t, J=7.0 Hz, 2H), 1.83 (m, 2H), 1.39 (m, 18H); 0.88 (m, J=6.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035004B2
Source datasetuspto-grants-2015_05
ORD IDord-b3c7173ef1534b90887d0c10e82ba97d
Source noteuspto-grants-2015_05