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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1738671생성일: 2026년 10월 26일

Triphenylphosphine → Ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-2-oxoacetate

https://huagongshe.com/reaction/1738671

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물tert-Butyl (3R)-3-hydroxypyrrolidine-1-carboxylateHCID 6544479—
반응물Ethyl 2-(4-hydroxyphenyl)-2-oxoacetateHCID 11715332—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-2-oxoacetateHCID 1031664175.1%

반응 단계

To 40 ml of tetrahydrofuran were dissolved 1.8 g of ethyl 2-(4-hydroxyphenyl)-2-oxoacetate, 1.74 g of (3R)-1-tert-butoxycarbonyl-3-hydroxypyrrolidine and 2.92 g of triphenylphosphine. At room temperature, 1.94 g of diethyl azodicarboxylate was added to the above solution, and the resulting mixture was stirred for 18 hours. After distilling off the solvent, the residue thus obtained was dissolved in ethyl acetate, and the solution was washed with water, and then dried. Thereafter, the solvent was distilled-off, and the resulting residue was purified by silica gel column chromatography using a toluene/chloroform mixture as an eluant, thereby obtaining 2.53 g of the title compound as a viscous yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05962695
출처 데이터셋uspto-grants-1999_10
ORD IDord-07fb540c4d3843f9a37e29578f463dce
출처 메모uspto-grants-1999_10