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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164717Generated: November 1, 2026

Tetrahydrofuran → HCID 20403098, compound

https://huagongshe.com/reaction/2164717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-3-methoxy-1,4-naphthalenedioneHCID 27459—
ReactantAluminum(III) ChlorideHCID 6451240—
CatalystZincchlorideHCID 3007855—
Product2-Chloro-3-dodecyl-1,4-naphthoquinoneHCID 1030504.6%
ProductHCID 20403098HCID 2040309812.3%

Reaction Steps

To 0.20 g (1.50 mmoles) of AlCl3 in 20 mL of THF was added 6.80 g (4.74 mmoles, 0.697 mmoles/g) of dodecyl MgBr. This mixture was added dropwise to 0.789 g (4.49 mmoles) of 2-methoxy-3-chloro-1,4-naphthoquinone and 0.529 g (3.89 mmoles) of ZnCl2 in 50 mL of THF. The mixture was stirred overnight. The green solution was poured into 100 mL of NH4Cl solution, extracted with 3×50 mL of ether, dried over MgSO4, filtered, and solvent was removed. The residue was flash-chromatographed (90% toluene/hexane as eluant) to give 0.075 g (0.021 mmoles, 4.6%) of 2-dodecyl-3-chloronaphthoquinone and 0.246 g (0.55 mmoles, 12.3%) of 2-dodecyl-3-methoxynaphthoquinone. 1H NMR (δ, CDCl3): 8.05 (m,2H), 7.65 (m,2H), 4.10 (s,3H), 2.55 (m,2H), 1.3 (br. s,20H), 0.85 (m,3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507241
Source datasetuspto-grants-1985_03
ORD IDord-0685d50eeab4447ca8edd889c3931111
Source noteuspto-grants-1985_03