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HRID 29281作成日:2026年10月24日

Ethyl Acetate → methyl N-[(4'-nitro-1,1'-biphenyl-4-yl)sulfonyl]-L-valinate

https://huagongshe.com/ja/reaction/29281

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium BicarbonateHCID 516892—
反応物4-Nitrophenylboronic acidHCID 2773552—
反応物methyl N-[(4-bromophenyl)sulfonyl]-L-valinateHCID 47337186—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物methyl N-[(4'-nitro-1,1'-biphenyl-4-yl)sulfonyl]-L-valinateHCID 1006907781%

反応手順

A mixture of 0.175 g (0.5 mmol) of methyl N-[(4-bromophenyl)sulfonyl]-L-valinate, 0.25 g (1.5 mmol) of 4-nitrophenylboronic acid, 0.087 g of tetrakis(triphenylphosphine)palladium and 8 mL of saturated sodium bicarbonate in 8 mL of ethylene glycol dimethyl ether were refluxed for 2 h, then cooled to room temperature. To the reaction was added 50 mL of ethyl acetate and 40 mL of water. The water layer was extracted with ethyl acetate. The combined ethyl acetate layers was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexane:ethyl acetate (2:1) to provide 0.159 g of methyl N-[(4′-nitro-1,1′-biphenyl-4-yl)sulfonyl]-L-valinate as a yellow solid. Yield 81%. m.p. 144-146° C.; MS: 391.0(M−H)−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420001B2
出典データセットuspto-grants-2008_09
ORD IDord-0a555bc7f2294e2684f21f1665cd84dc
出典メモuspto-grants-2008_09