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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 558414생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/558414

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물alpha-Bromo-o-fluorotolueneHCID 67968—
반응물Ethyl 3-formyl-4-methoxybenzoateHCID 638670—
반응물Sodium MethoxideHCID 10942334—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 3-[2-(2-fluorophenyl)-vinyl]-4-methoxybenzoateHCID 6700208580%

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063046B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-184780b3ef50493d9036ea9668845aed
출처 메모uspto-grants-2011_11