돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17875생성일: 2026년 10월 24일

Triphenylphosphine → 1-oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/17875

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물BenzenepropanolHCID 31234—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid ethyl esterHCID 11845279—
용매TetrahydrofuranHCID 8028—
생성물1-oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carboxylic acid ethyl esterHCID 1184528285%

반응 단계

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (1.7 g, 6.07 mmol), 3-phenylpropanol (1.65 g, 12.14 mmol) and triphenylphosphine (3.18 g, 12.14 mmol) were dissolved in tetrahydrofuran (100 ml). Diethyl azodicarboxylate (2 ml, 12.14 mmol) dissolved in tetrahydrofuran (20 ml) was added dropwise thereto at 0° C. After stirring for 6 hours at room temperature, the mixture was washed with brine, extracted with ethyl acetate, the extract was dried over anhydrous magnesium sulfate, the concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (diethyl ether:hexane=1:10) to obtain the title compound (yield 85%) as a dark red solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741323B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b01a65d8d7f7470f9c3b2f407b55bba8
출처 메모uspto-grants-2010_06