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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358362Generated: October 29, 2026

Thiophenol → HCID 86739140, compound

https://huagongshe.com/reaction/358362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium HydroxideHCID 14797—
Reactant1,4-Naphthalenedione, 5-amino-2,3-dimethoxy-HCID 12250696—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 86739140HCID 86739140—

Reaction Conditions

Temperature5 °C

Reaction Steps

Sodium nitrite (0.18 g) was added at 0°-5° C. to a stirred suspension of 5-amino-2,3-dimethoxy-1,4-naphthoquinone (233 mg, 1 mmol) in 0.6N hydrochloric acid (10 ml) and tetrahydrofuran (1 ml). The mixture was stirred at 5° C. for 10 minutes until a clear solution was obtained and was then neutralized by the addition of sodium carbonate. The ice cold solution was then slowly added to a vigorously stirred two-phase mixture in a nitrogen atmosphere at 50° C. composed of potassium hydroxide (0.16 g), water (10 ml), thiophenol (0.32 ml) and ethyl acetate (35 ml). After a total reaction time of 20 min, the mixture was partitioned between ethyl acetate (40 ml) and brine (100 ml). The ethyl acetate phase was dried over MgSO4 and concentrated in vacuo. The residue was purified by chromatography on a thick layer silica gel plate using acetone:toluene:chloroform (1:20:20) giving a solid that, after recrystallizing from isopropanol, afforded 70 mg of 2,3-dimethoxy-5-phenylthio-1,4-naphthoquinone, mp 76°-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04466981
Source datasetuspto-grants-1984_08
ORD IDord-c61e5b14ff7d4e70bd209cb687905634
Source noteuspto-grants-1984_08