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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428320생성일: 2026년 10월 24일

Vinyl isobutyl ether → HCID 54165959, 화합물

https://huagongshe.com/ko/reaction/428320

반응식

참여 물질

역할이름HCID투입량
반응물Vinyl isobutyl etherHCID 7992—
반응물TriethylamineHCID 8471—
반응물1,3-Bis(diphenylphosphino)propaneHCID 81219—
반응물(R)-3-(2-benzyloxy)-5-bromophenyl)-N,N-diisopropyl-3-phenylpropan-1-amineHCID 24885301—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물HCID 54165959HCID 54165959—

반응 조건

온도100 °C

반응 단계

To a stirred solution of (R)-N,N-diisopropyl-3-(2-benzyloxy-5-bromophenyl)-3-phenylpropanamine (Example 12) (10.2 g, 21.23 mmol) in DMF (100 mL) under nitrogen atmosphere at room temperature were sequentially added triethylamine (2.58 g, 25.47 mmol), TlOAc (6.15 g, 23.35 mmol), isobutylvinylether (14 mL, 106.14 mmol), DPPP (0.87 g, 2.12 mmol) and Pd(OAc)2 (0.24 g, 1.06 mmol). The reaction temperature was raised to 100° C. and stirred for 3 hours, cooled to room temperature, filtered and treated with HCl (5%, 250 mL) and stirred for another 2 hours. The reaction mixture was repeatedly extracted with dichloromethane and the combined organic layers were dried (MgSO4), filtered and the solvent evaporated. Triethylamine and DMF were destined off under reduced pressure to yield 9 g (98%); 1H NMR (CDCl3) δ1.22 (m, 12H), 2.52-2.70 (m, 7H), 3.40 (br, 2H), 4.34 (t, 1H), 5.10 (s, 1H), 6.90 (d, 1H), 7.17-7.40 (m, 10H), 7.82 (m, 1H) and 7.92 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313132B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-1c4499c960ae4932a4e9ac8d078bc00c
출처 메모uspto-grants-2001_11