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HRID 370294作成日:2026年10月26日

Diisopropylaniline → Propylbenzene

https://huagongshe.com/reaction/370294

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylanilineHCID 32484—
反応物4,4'-DifluorobenzilHCID 123072—
触媒Titanium TetrachlorideHCID 24193—
溶媒BenzeneHCID 241—
生成物PropylbenzeneHCID 7668—

反応条件

温度2 °C

反応手順

In a 250--mL RB flask fitted with pressure equalizing addition funnel, thermometer, magnetic stirrer, and N2 inlet was placed 0.75 g (3.0 mmol) of 4,4'-difluorobenzil, 13.8 mL (80 mmol) of 2,6-diisopropylaniline (DIPA), and 100 mL dry benzene. In the addition funnel was placed 50 mL of dry benzene and 210 mL (3.5 g; 18 mmol) of titanium tetrachloride. The reaction flask was cooled to 2° C. with ice and the TiCl4 solution was added dropwise over 45 min, keeping the reaction temperature below 5° C. The ice bath was removed after addition was complete and the mixture was stirred at RT for 72 h. The reaction mixture was partitioned between water and ethyl ether, and the ether phase was rotovapped and the concentrated oil was washed with 800 mL 1N HCl to remove the excess diisopropylaniline. The mixture was extracted with 100 mL of ether, and the ether layer was washed with water and rotovapped. Addition of 15 mL hexane plus 30 mL of methanol to the concentrate resulted in the formation of fine yellow crystals which were filtered, methanol-washed, and dried under suction to yield 0.4 g of (2,6--i--PrPh)2DAB(4--F--Ph)2, mp: 155°-158° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06140439
出典データセットuspto-grants-2000_10
ORD IDord-f6a9810ca5a34be3a064857afd9b7fe0
出典メモuspto-grants-2000_10