돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413934생성일: 2026년 10월 26일

Tributylphosphine → (E)-(S)-2-ethoxy-3-[4-(3-methyl-5-phenyl-pent-2-en-4-ynyloxy)-phenyl]-propionic acid ethyl ester

https://huagongshe.com/reaction/413934

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물Ethyl (2S)-2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 9816147—
반응물(E)-3-methyl-5-phenyl-pent-2-en-4-yn-1-olHCID 10797282—
용매BenzeneHCID 241—
생성물(E)-(S)-2-ethoxy-3-[4-(3-methyl-5-phenyl-pent-2-en-4-ynyloxy)-phenyl]-propionic acid ethyl esterHCID 1020053870.3%

반응 단계

The title compound was prepared from of (E)-3-methyl-5-phenyl-pent-2-en-4-yn-1-ol (0.172 g, 1.0 mmol), (J. Med. Chem. 1998, 41(14), 2524-2536), tributylphosphine (0.370 mL, 1.5 mmol), 1,1′-(azodicarbonyl)dipiperidine (0.378 g, 1.5 mmol) and (S)-ethyl 2-ethoxy-3-(4-hydroxy-phenyl)-propionate (0.262 g, 1.1 mmol) in dry benzene (20 mL) by a procedure analogous to that described in example 3, yielding 0.276 g (68%) of (E)-(S)-2-ethoxy-3-[4-(3-methyl-5-phenyl-pent-2-en-4-ynyloxy)-phenyl]-propionic acid ethyl ester. 1H NMR (300 MHz, CDCl3) δ: 1.1-1.25 (6H, m), 1.98 (3H, d), 2.95 (2H, d), 3.29-3.4 (1H, m), 3.53-3.65 (1H, m), 3.95 (1H, t), 4.15 (2H, q), 4.60 (2H, dd), 6.15 (1H, dt), 6.8 (2H, d), 7.15 (2H, d), 7.20-7.3 (3H, m), 7.35-7.45 (2H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06569901B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-b37fdb078e2346d7b05aa2df048830ea
출처 메모uspto-grants-2003_05