戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 381842作成日:2026年10月27日

Triethylamine → 4-(4'-Cyano-biphenyl-4-yl)4-oxo-butyric acid, methyl ester

https://huagongshe.com/reaction/381842

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methyl 4-(4-bromophenyl)-4-oxobutanoateHCID 838865—
反応物4-Cyanophenylboronic acidHCID 2734326—
触媒palladium(II) acetateHCID 167845—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物4-(4'-Cyano-biphenyl-4-yl)4-oxo-butyric acid, methyl esterHCID 2175170958.6%

反応条件

温度105 °C

反応手順

A stirred mixture of (4-cyano-phenyl)boronic acid (0.220 g, 0.00150 mol), 4-(4-bromo-phenyl)-4-oxo-butyric acid, methyl ester (0.2715 g, 0.00100 mol), triethylamine (0.418 mL, 0.0030 mol), tri(O-toluyl)phosphine (0.0191 g, 0.0000628 mol) and palladium(II)acetate (0.0067 g, 0.000030 mol) in dry dimethylformamide (4.0 mL) was heated at 105° C. under nitrogen for 2 hours and allowed to cool. For convenience, allowed to stand overnight. The mixture was diluted with diethyl ether, and the resulting suspension was filtered through Celite. The Celite and filtercake were washed with additional diethyl ether then dichloromethane. The filtrate and washings were combined and washed with 0.5 M aqueous hydrochloric acid, water, 3% aqueous ammonium hydroxide, water, and brine. The organics were dried (Na2SO4) and rotary evaporated. The residue was dissolved (chloroform) and chromatographed on silica gel (35 g, 230-400 mesh), eluting with hexanes-acetone (4:1, 30×30 mL) to give 0.172 g of 4-(4′-cyano-biphenyl-4-yl)-4-oxo-butyric acid, methyl ester as a pale yellow solid; mp 149-151° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06307089B2
出典データセットuspto-grants-2001_10
ORD IDord-320f05eec1b64f479fe60781f1d2309d
出典メモuspto-grants-2001_10