HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481102Generated: October 29, 2026
3-Fluoroaniline → HCID 18766887, compound
https://huagongshe.com/reaction/481102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluoroaniline | HCID 9742 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 20605628 | HCID 20605628 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18766887 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06653471B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-1d710dcaa20a4c0981a3c6b62f7c30d5 |
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| Source note | uspto-grants-2003_11 |
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