돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 381842생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/381842

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl 4-(4-bromophenyl)-4-oxobutanoateHCID 838865—
반응물4-Cyanophenylboronic acidHCID 2734326—
촉매palladium(II) acetateHCID 167845—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물4-(4'-Cyano-biphenyl-4-yl)4-oxo-butyric acid, methyl esterHCID 2175170958.6%

반응 조건

온도105 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06307089B2
출처 데이터셋uspto-grants-2001_10
ORD IDord-320f05eec1b64f479fe60781f1d2309d
출처 메모uspto-grants-2001_10