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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084455Generated: October 31, 2026

4-Fluoroaniline → HCID 20063357, compound

https://huagongshe.com/reaction/1084455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroanilineHCID 9731—
ReactantHCID 20063336HCID 20063336—
SolventDiethyl EtherHCID 3283—
ProductHCID 20063357HCID 20063357—

Reaction Steps

A suspension of 4-isopropylisocoumarin-3-carboxylic acid (24.68 g) in 4-fluoroaniline (74 ml) was refluxed under argon for 15 minutes. After cooling, the reaction mixture was dissolved in diethyl ether and the resulting solution extracted with aqueous sodium hydroxide (3×300 ml; 1M). The combined aqueous phases were washed with diethyl ether and acidified to pH1 with aqueous hydrochloric acid (2M). The resultant precipitate was filtered, washed with water and dried at 100° C. to give 2-(4-fluorophenyl)-4-isopropyl-1-oxo-1,2-dihydroisoquinoline-3-carboxylic acid (25.2 g) in the form of a white solid, m.p. 276°-277° C. (with decomposition) [Elemental analysis: C, 69.9; H, 4.9; N, 4.3%; calculated: C, 70.15; H, 4.9; N, 4.3%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004747
Source datasetuspto-grants-1991_04
ORD IDord-5a1b2cdff38e4064a0320834c623d5df
Source noteuspto-grants-1991_04