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HRID 222847作成日:2026年10月26日

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

https://huagongshe.com/reaction/222847

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物tert-Butyl diethylphosphonoacetateHCID 2773685—
反応物Methyl 4-formyl-2-methoxybenzoateHCID 18510332—
反応物Sodium t-butoxideHCID 23676156—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-((e)-2-tert-butoxycarbonyl-vinyl)-2-methoxy-benzoateHCID 23282641—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207373B2
出典データセットuspto-grants-2012_06
ORD IDord-77ea7f73f1194be8b1358c6d06576aa5
出典メモuspto-grants-2012_06