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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422573Generated: November 1, 2026

Boron trifluoride → HCID 136389335, compound

https://huagongshe.com/reaction/2422573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantSodium HydroxideHCID 14798—
Reactant4(3H)-Quinazolinone, 2-(4-methoxyphenyl)-3,8-dimethyl-HCID 67244592—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 136389335HCID 13638933580.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-(4-Methoxyphenyl)-3,8-dimethyl-4(3H)-quinazolinone (2.02 g, 7.20 mmol) was dissolved in dichloromethane (10 ml), stirred at −78° C., then boron trifluoride (1.0 M in CH2 Cl2, 21.6 ml) was added thereto, gradually heated up to room temperature, and stirred at that temperature for 12 hours. The reaction solution was diluted with ethyl acetate, and with cooling with ice, this was poured into aqueous 1 N sodium hydroxide solution, and extracted with ethyl acetate. The organic layer was washed with 1 N hydrochloric acid and saturated saline water, and dried with magnesium sulfate. The organic layer was concentrated under reduced pressure to obtain the intended compound (1.54 g, 80%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960394B2
Source datasetuspto-grants-2011_06
ORD IDord-9ee45a0b7a5840cf85aa0ff80a6626d5
Source noteuspto-grants-2011_06