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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904711Generated: October 31, 2026

Thiophenol → HCID 86739140, compound

https://huagongshe.com/reaction/904711

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 Steps

Sodium nitrite (0.18 g) is added at 0°-5° to a stirred suspension of 5-amino-2,3-dimethoxy-1,4-naphthoquinone (233 mg, 1 mmol) in 0.6 N hydrochloric acid (10 ml) and tetrahydrofuran (1 ml). The mixture is stirred at 5° for 10 minutes until a clear solution is obtained and is then neutralized by the addition of sodium carbonate. The ice cold solution is then slowly added to a vigorously stirred two-phase mixture in a nitrogen atmosphere at 50° 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 is partitioned between ethyl acetate (40 ml) and brine (100 ml). The ethyl acetate phase is dried over MgSO4 and concentrated in vacuo. The residue is 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, affords 70 mg of 2,3-dimethoxy-5-phenylthio-1,4-naphthoquinone, mp 76°-77°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04419368
Source datasetuspto-grants-1983_12
ORD IDord-707fa44dc8dc45ca85472d220996d16d
Source noteuspto-grants-1983_12