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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193821Generated: October 28, 2026

Water → 4,4-Dioctyl-4H-cyclopenta[2,1-b:3,4-b']dithiophene

https://huagongshe.com/reaction/2193821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantDichloromethaneHCID 6344—
Reactant9-([2,2'-Bithiophen]-3-yl)heptadecan-9-olHCID 58568000—
SolventOctaneHCID 356—
Product4,4-Dioctyl-4H-cyclopenta[2,1-b:3,4-b']dithiopheneHCID 59582544—

Reaction Steps

H2SO4 (9.38 mL) was added dropwise to 9-([2,2′-bithiophen]-3-yl)heptadecan-9-ol (IIe) (6.20 g, 15 mmol) in 200 ml n-octane under stirring at room temperature. After stirring for 12 h, CH2Cl2 (130 mL) and water (130 mL) were added. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined organic extracts were successively washed with saturated NaHCO3 and brine. After drying over MgSO4, the solvent was removed in vacuo. The crude oil was purified with column chromatography (eluent hexane) to afford a pure dark yellow oil (Ie) (3.19 g, 52.9%). 1H-NMR (CDCl3): δ=7.14 (d, J=4.8 Hz, 2H), 6.93 (d, J=5.1 Hz, 2H), 1.87-1.79 (m, 4H), 1.40-1.06 (m, 24H), 0.95-0.82 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329923B2
Source datasetuspto-grants-2012_12
ORD IDord-18d009546e0b4b0fa18a90103f7b2441
Source noteuspto-grants-2012_12