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HRID 558414作成日:2026年10月27日

Triphenylphosphine → Ethyl 3-[2-(2-fluorophenyl)-vinyl]-4-methoxybenzoate

https://huagongshe.com/reaction/558414

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物alpha-Bromo-o-fluorotolueneHCID 67968—
反応物Ethyl 3-formyl-4-methoxybenzoateHCID 638670—
反応物Sodium MethoxideHCID 10942334—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 3-[2-(2-fluorophenyl)-vinyl]-4-methoxybenzoateHCID 6700208580%

反応条件

温度80 °C

反応手順

N,N-Dimethylformamide (5 mL) was added to 1.0 g of polymer-supported triphenylphosphine (produced by Fluka, CAS registry number 39319-11-4) and 1.1 g of 2-fluorobenzyl bromide, and the mixture was stirred for 10 hours at 80° C. The reaction mixture was filtered, and then washed with N,N-dimethylformamide, dichloromethane, and methanol. The residue was dried under reduced pressure to prepare polymer-supported (2-fluorobenzyl)-triphenylphosphonium bromide. This product (144 mg) was added to a methanol solution (2 mL) of 30 mg of ethyl 3-formyl-4-methoxybenzoate obtained in step C of Example 1-2-1. After 80 μL of 28% sodium methoxide was added, the reactor was sealed, and the mixture was stirred for 4 hours at 70° C. The residue was diluted with ethyl acetate, washed with purified water, and dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was separated by filtration, and then the filtrate was concentrated under reduced pressure. The residue was dried under reduced pressure to obtain 33 mg (80%) of ethyl 3-[2-(2-fluorophenyl)-vinyl]-4-methoxybenzoate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063046B2
出典データセットuspto-grants-2011_11
ORD IDord-184780b3ef50493d9036ea9668845aed
出典メモuspto-grants-2011_11