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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195100Generated: November 2, 2026

Sodium Hydroxide → HCID 59609194, compound

https://huagongshe.com/reaction/2195100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(Benzo(1,2-b:4,5-b)dithiophene-4,8-dione)HCID 288478—
ReactantHCID 4277813HCID 4277813—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 59609194HCID 59609194—

Reaction Steps

Benzo[1,2-b:4,5-b′]dithiophene-4,8-dione (1.0 g, 4.54 mmol) and Zn powder (0.659 g, 10.1 mmol) were suspended in ethanol (10 mL). A solution of NaOH (3 g) in water (15 mL) was added. The resulting mixture was heated to reflux for 1 hour, after which 2-hexyldecyl(4-methylbenzenesulfonate) (3.86 g, 9.73 mmol) was added. The reaction was heated to reflux overnight. The reaction was cooled to room temperature and water (50 mL) was added. The reaction was extracted with ether, followed by separation and drying of the organic layer over MgSO4. Solvent was removed and the residue was purified by chromatography (10% dichloromethane in hexanes as eluent). The yield of the 4,8-bis[(2-hexyldecyl)oxy]-benzo[1,2-b:4,5-b′]dithiophene was 0.80 g (26%). 1H NMR (CDCl3, 500 MHz) δ=7.47 (d, J=2.75, 2H), 7.36 (d, J=2.75, 2H), 4.16 (m, 4H), 1.86 (m, 2H), 1.38-1.65 (m, 48H), 0.86 (m, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334456B2
Source datasetuspto-grants-2012_12
ORD IDord-a87e544db3c7475ab46ddebb6c97023a
Source noteuspto-grants-2012_12