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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593631Generated: October 31, 2026

Ammonium → 6-Fluoro-2,3,4,9-tetrahydro-1H-carbazole-3-carboxylic acid

https://huagongshe.com/reaction/1593631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniumHCID 223—
ReactantSodium HydroxideHCID 14798—
Reactant4-Fluorophenylhydrazine hydrochlorideHCID 69981—
ReactantEthyl 4-oxocyclohexanecarboxylateHCID 317638—
SolventEthanolHCID 702—
Product6-Fluoro-2,3,4,9-tetrahydro-1H-carbazole-3-carboxylic acidHCID 2154835497.5%

Reaction Conditions

Temperature62.5 °C

Reaction Steps

In a 5-L cylindrical reactor, p-fluorophenylhydrazine HCl (400 g, 2.46 mol) was suspended in ethanol (2B) (1.2 kg; 1.5 L). The slurry was stirred and heated to 60-65° C. A solution of 4-cyclohexanone carboxylic acid ethyl ester (400 g, 2.35 mol) in ethanol (2B) (0.4 L) was added over 1 h. The reaction temperature may rise to reflux (78-82° C.). After addition, the suspension was stirred and heated at reflux for 1 h then cooled to 40-50° C. A 50% sodium hydroxide solution (470 g) was added over 30 min. The suspension was heated to reflux (80-82° C.). (This can cause evolution of ammonium gas during heating). After 1 h, the reaction mixture was distilled at atmospheric pressure to about 1.5 L, about half of its original volume, then cooled to 60-70° C. Water (2.5 L) was added. The mixtured was cooled to 30-40° C. before dilute HCl (0.333 L conc HCl+0.667 L water) was added over 20 min. The suspension was stirred at 20° C. for 1 h then filtered through a Buchner funnel. The solid product was washed with water (3×1 L) then dried under N2 overnight to give 534.5 g (97.5% yield) of off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297704B2
Source datasetuspto-grants-2007_11
ORD IDord-2590631be7de4b7cb72b8d3932882f85
Source noteuspto-grants-2007_11