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HRID 1474493作成日:2026年10月26日

Hydroxyphenylacetic acid → 2,4,4'-Trihydroxydeoxybenzoin

https://huagongshe.com/reaction/1474493

反応式

関与物質

役割名称HCID仕込み量
反応物Hydroxyphenylacetic acidHCID 127—
反応物ResorcinolHCID 5054—
反応物Boron trifluoride etherateHCID 8000—
反応物Sodium AcetateHCID 517045—
溶媒TolueneHCID 1140—
生成物2,4,4'-TrihydroxydeoxybenzoinHCID 64009687%

反応条件

温度108 °C

反応手順

Resorcinol (1,3-dihydroxybenzene) (62.000 g, 563.1 mmol, 1.0 equiv.) and 4-Hydroxyphenylacetic acid (94.237 g, 619.4 mmol, 1.1 equiv.) were added to a 3 neck 2 L round bottomed flask fitted with a paddle, a pressure equalizing addition funnel and a thermometer and a heating mantle. Toluene (350 mL) was added to the flask to give a suspension. The reaction purged with nitrogen and the addition funnel filled with Boron trifluoride etherate (198.201 ml, 1578.0 mmol, 2.8 equiv.) via canula. The reaction was stirred at 150 rpm and boron trifluoride etherate was added in portions of 3-4 mL and the reaction heated. During addition the internal temperature rose to 100° C. The reaction went through various changes in color from yellow to dark red. After complete addition of boron trifluoride etherate the addition funnel was removed and replaced with a condenser. The reaction was stirred for 1.5 h at an internal temperature of 108° C. A sample was taken and HPLC analysis indicated the reaction was complete. The reaction was cooled and stirring stopped to give a biphasic solution. A 12% aqueous solution of sodium acetate (41 g, 336 mL) was slowly added to the reaction with stirring. The reaction was stirred for 16 hours. A precipitate formed overnight and was collected in a sintered glass funnel. The solid was dried on a vacuum oven for 16 h to give the product as a white powder (119.67 g, 87.0%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09018244B2
出典データセットuspto-grants-2015_04
ORD IDord-dea33d26cc804f5b9a1e77c83ccda1c0
出典メモuspto-grants-2015_04