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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322871생성일: 2026년 10월 24일

Triphenylphosphine → methyl (RS)-5-[3-(3-methyl-2-thienylmethoxy)phenyl]-4-(2-methylphenyl)-5-oxopentanoate

https://huagongshe.com/ko/reaction/322871

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물methyl (RS)-5-(3-hydroxyphenyl)-5-oxo-4-(2-methylphenyl)pentanoateHCID 10805064—
반응물(3-Methylthiophen-2-yl)methanolHCID 12875263—
용매TetrahydrofuranHCID 8028—
생성물methyl (RS)-5-[3-(3-methyl-2-thienylmethoxy)phenyl]-4-(2-methylphenyl)-5-oxopentanoateHCID 2320427738.6%

반응 조건

온도5 °C

반응 단계

A solution of triphenylphosphine (1.13 g) in tetrahydrofuran (30 mL) is treated with diisopropyl azodicarboxylate (0.84 mL) at 0-5° C. The suspension is then treated with methyl (RS)-5-(3-hydroxyphenyl)-5-oxo-4-(2-methylphenyl)pentanoate (671 mg) and 3-methyl-2-thienylmethanol (275 mg), and stirred at 5° C. for 15 minutes. The solution is evaporated and the residue is subjected to flash chromatography on silica gel, eluting with a mixture of pentane and ethyl acetate (5:1 v/v), to give methyl (RS)-5-[3-(3-methyl-2-thienylmethoxy)phenyl]-4-(2-methylphenyl)-5-oxopentanoate (350 mg), in the form of an oil. [NMR(CDCl3):- 2.0-2.5(4H,m), 2.25(3H,s),2.5(3H,s), 3.65(3H,s), 4.8(1H,m),5.1 (2H,q),6.85-7.5(10H)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211234B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-7d6ff9da47ce431188d4f1f50ec7c1a9
출처 메모uspto-grants-2001_04