HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986648Generated: October 30, 2026
Boron trifluoride etherate → HCID 13376462, compound
https://huagongshe.com/reaction/986648
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | N-(2,4-Dimethylphenyl)-2-(2-fluoroacetamido)-5-nitrobenzamide | HCID 13376455 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13376462 | HCID 13376462 | 68.6% |
Reaction Steps
4.0 g of N-(2-fluoroacetamido-5-nitrobenzoyl)-2,4-dimethylaniline are added to a mixture of 30 ml of acetic acid and 3.5 g of boron trifluoride etherate, and the mixture is stirred under heating at 100° to 105° C. for 30 minutes. The mixture is cooled and concentrated under reduced pressure to remove acetic acid. 50 ml of water are added to the residue, and the mixture is neutralized with potassium carbonate. The mixture is extracted with chloroform, and the extract is washed with water and dried. The chloroform solution is concentrated under reduced pressure to remove solvent. Isopropanol is added to the residue, and crystalline precipitates are collected by filtration. The thus-obtained crystals (3.0 g, M.p. 198°-200° C.) are recrystallized from a mixture of dimethylformamide and ethanol (1:2). 2.6 g of 2-fluoromethyl-3-(2,4-dimethylphenyl)-6-nitro-4(3H)-quinazolinone are obtained as colorless prisms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04714702 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-f54607b876304902882ff3970af90296 |
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| Source note | uspto-grants-1987_12 |
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