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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481102Generated: October 29, 2026

3-Fluoroaniline → HCID 18766887, compound

https://huagongshe.com/reaction/481102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluoroanilineHCID 9742—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 20605628HCID 20605628—
SolventDichloromethaneHCID 6344—
ProductHCID 18766887HCID 18766887—

Reaction Steps

To a solution of 0.38 mL (4 mmol) of 3-fluoroaniline in 2 mL of methylene chloride under a nitrogen atmosphere is added dropwise 1.5 mL (3 mmol) of trimethyl aluminum (2M solution of toluene). This mixture is stirred at room temperature for 30 minutes. To this mixture is added a solution of 0.12 g (0.5 mmol) of 3,4,5,6-tetrahydro-3,5,10-triaza-benzo(e)azulene-1-carboxylic acid methyl ester dissolved in 8 mL of methylene chloride. The reaction mixture is heated to 40° C. for 24 hours; cooled to room temperature and quenched with 0.5 mL of saturated NaCl. After stirring for 30 minutes an additional 5 mL of methylene chloride and 2 grams of anhydrous sodium sulfate is added. The reaction mixture is filtered. The filtrate is evaporated and chromatographed on 10 grams of silica gel using 10/1/0.5 chloroform/methanol/ammonium hydroxide as the eluant. Appropriate fractions are combined and evaporated to 23 mg of 3,4,5,6-tetrahydro-3,5,10-triaza-benzo(e)azulene-1-carboxylic acid (3-fluoro-phenyl)-amide. 1H NMR (CD3OD) δ8.70 (m, 1H), 7.90 (m, 1H), 7.80 (m, 1H), 7.60 (s, 1H), 7.30 (m, 3H), 6.90 (m, 1H), 3.87 (s, 2H), 3.70 (s, 2H). Mass spectrum: m/e=323.2 (p+1). TLC (10/1/0.1 chloroform/methanol/ammonium hydroxide) Rf=0.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653471B2
Source datasetuspto-grants-2003_11
ORD IDord-1d710dcaa20a4c0981a3c6b62f7c30d5
Source noteuspto-grants-2003_11