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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385199Generated: October 31, 2026

Sulfuric Acid → HCID 15345813, compound

https://huagongshe.com/reaction/1385199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDiethyl EtherHCID 3283—
Reactant2-Amino-3-chloro-1,4-naphthoquinoneHCID 17748—
Reactant3-Fluorobenzoyl chlorideHCID 74376—
SolventNitrobenzeneHCID 7416—
ProductHCID 15345813HCID 153458137.1%

Reaction Steps

To a solution of 5.00 g (24 mmol) of 2-amino-3-chloro-1,4-dihydro-1,4-dioxonaphthalene in 50 mL of nitrobenzene, 14.6 mL (120 mmol) of 3-fluorobenzoic acid chloride are added; after 5 min of stirring, 0.50 mL of concentrated sulfuric acid is then added with protection from light. After 24 h of reflux and complete cooling, 200 mL of ether are added to the reaction mixture. The precipitate formed is filtered, then redissolved in 200 mL of dichloromethane, to which 100 mL of a glacial sodium hydroxide solution are added. After 6 h of stirring at this temperature, the organic phase is extracted, washed several times with water and dried over calcium chloride. The solid obtained after evaporation of the solvent is purified on a medium-pressure column (support: silica; conditioning heptane; eluant: dichloromethane/heptane, 50/50). The yellow crystals so obtained are uncolored and recrystallized in a dichloromethane/heptane mixture (volume/volume) to produce 0.50 g of 4,9-dihydro-4,9-dioxo-2-(3-fluorophenyl)-naphtho[2,3-d]oxazole in the form of yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262095B1
Source datasetuspto-grants-2001_07
ORD IDord-384762032c62428e9441e44058c6b133
Source noteuspto-grants-2001_07