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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385206Generated: October 31, 2026

Acetic Acid → HCID 15345817, compound

https://huagongshe.com/reaction/1385206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium SulfideHCID 14804—
Reactant2-Amino-3-chloro-1,4-naphthoquinoneHCID 17748—
Reactanto-FluorobenzaldehydeHCID 67970—
SolventWaterHCID 962—
ProductHCID 15345817HCID 1534581727%

Reaction Steps

To a suspension of 5.0 g (24 mmol) of 2-amino-3-chloro-1,4-dihydro-1,4-dioxonaphthalene in 80 mL of water, 8.4 g (35 mmol) of nonahydrated sodium sulfide are added. The reaction mixture is then heated to reflux for approximately 20 min, then 20 mL of an aqueous solution containing 2.0 g of sodium sulfide are added. When the color of the medium has completely changed to blue, 1.95 mL (24 mmol) of 2-fluorobenzaldehyde and 6.36 mL of glacial acetic acid are added successively. After 1 h of reflux, the black semisolid product obtained is filtered, dried, and purified on a flash column (support: silica; conditioning: heptane; eluant: dichloromethane/heptane, 50/50). The greenish crystals formed after evaporation of the solvent are washed several times with ethanol and ether, then they are uncolored and recrystallized in dichloromethane to produce 2.0 g of 4,9-dihydro-4,9-dioxo-2-(2-fluorophenyl)-naphtho[2,3-d]thiazole in the form of yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262095B1
Source datasetuspto-grants-2001_07
ORD IDord-57d5bb3c73824199a425c89e1f19e300
Source noteuspto-grants-2001_07