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HRID 222847생성일: 2026년 10월 25일

Ammonium Chloride → Methyl 4-((e)-2-tert-butoxycarbonyl-vinyl)-2-methoxy-benzoate

https://huagongshe.com/reaction/222847

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물tert-Butyl diethylphosphonoacetateHCID 2773685—
반응물Methyl 4-formyl-2-methoxybenzoateHCID 18510332—
반응물Sodium t-butoxideHCID 23676156—
용매TetrahydrofuranHCID 8028—
생성물Methyl 4-((e)-2-tert-butoxycarbonyl-vinyl)-2-methoxy-benzoateHCID 23282641—

반응 조건

온도0 °C

반응 단계

To 720 μL of tert-butyl diethylphosphonoacetate (1.1 equivalents) in 3 mL of tetrahydrofurane cooled to 0° C. under an inert atmosphere are added 307 mg of sodium tert-butanolate (1.15 equivalents). The whole is stirred for 30 minutes at 0° C. and then for 1 hour at room temperature. A solution cooled to 0-4° C. of 540 mg of aldehyde obtained in stage 3 in 1 ml of tetrahydrofurane is added dropwise to the previous mixture also cooled to 0° C. Stirring is maintained at this temperature for 30 minutes before letting the temperature rise back to room temperature for 2 hours. The medium is hydrolyzed with a saturated solution of ammonium chloride and extracted with ethyl acetate several times. The collected organic phases are washed with water, and then dried on magnesium sulfate, filtered and evaporated under reduced pressure. The reaction crude product is purified by chromatography on silica gel (petroleum ether/ethyl acetate: 95/5) leading to 500 mg of the expected product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207373B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-77ea7f73f1194be8b1358c6d06576aa5
출처 메모uspto-grants-2012_06