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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078756Generated: November 1, 2026

1,4-Dichlorobenzene → 1,4-Didodecylbenzene

https://huagongshe.com/reaction/2078756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DichlorobenzeneHCID 4685—
ReactantHCID 178443215HCID 178443215—
CatalystHCID 178418745HCID 178418745—
SolventDiethyl EtherHCID 3283—
Product1,4-DidodecylbenzeneHCID 15597206—

Reaction Steps

n-Dodecylmagnesium bromide (235 mL, 235.0 mmol, 1.0 M in diethyl ether) was added dropwise over 15 minutes, to a solution of 1,4-dichlorobenzene (15.00 g, 102.0 mmol) and [1,3-bis(diphenylphosphino)propane]nickel(II)chloride ((dppp)Cl2Ni, 70 mg) in dry ether (70 mL) at 0° C. The reaction mixture was subsequently allowed to warm to room temperature for about 30 minutes, heated under reflux for 1 day, and cooled to 0° C. again. The reaction was carefully quenched with water (10 mL) and HCl (70 mL, 2 M) and the aqueous layer was extracted with ether (2×50 mL). The combined organic layers were washed with water (30 mL), dried over MgSO4, and filtered. The solvent was then removed in vacuo and the crude product was heated to 100° C. under high vacuum (˜20 mtorr) for 10 hours to remove n-octane and n-octylbromide. 1,4-Di-n-dodecylbenzene (1) was obtained as a white solid (35.00 g, 83%). 1H NMR (CDCl3): δ 0.88 (t, 6H), 1.30 (m, 36H), 1.61 (m, 4H), 2.59 (t, 4H), 7.10 (s, 4H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928249B2
Source datasetuspto-grants-2011_04
ORD IDord-1d7c254d46a24e879ad33ca8d5d4a395
Source noteuspto-grants-2011_04