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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275543Generated: November 2, 2026

Quinone → 6-Methyl-1,4-naphthoquinone

https://huagongshe.com/reaction/1275543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinoneHCID 4650—
ReactantIsopreneHCID 6557—
ReactantChromic AcidHCID 24425—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product6-Methyl-1,4-naphthoquinoneHCID 59901231.8%

Reaction Steps

A solution of 1,4-benzoquinone (13.9 g, 128 mmol) and isoprene (13.1 ml, 131 mmol) was stirred in glacial acetic acid (44 ml) for 68 hours at room temperature. The mixture was diluted with water (44 ml) and refluxed for 11/2 hours. The mixture was cooled to room temperature and acetic acid (84 ml) and chromic acid [chromium trioxide (29.4 g) in water (30 ml)] was added sequentially, before refluxing for a further 11/2 hours. After cooling, the mixture was diluted with water (200 ml) and extracted with ether (3×50 ml). The combined ether fractions were washed with dilute sodium hydroxide solution (2M; 2 15×50 ml), water (2×50 ml), saturated sodium chloride solution (50 ml) and dried over magnesium sulphate. Filtration and evaporation of solvent under reduced pressure, and repeated recrystallisation from petroleum ether yielded the title compound (7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162799
Source datasetuspto-grants-2000_12
ORD IDord-b0c2a1797b624a4088ecb47321fc129b
Source noteuspto-grants-2000_12