7,8-Bis-(1,1-dimethyl-prop-2-ynyloxy)-2-phenyl-chromen-4-one → HCID 59052280, 화합물

HRID 734189노트

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HRID 734189 반응식
[CH3:1][C:2]([CH3:29])([O:5][C:6]1[C:15]([O:16][C:17]([CH3:21])([CH3:20])[C:18]#[CH:19])=[C:14]2[C:9]([C:10](=[O:28])[CH:11]=[C:12]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[O:13]2)=[CH:8][CH:7]=1)[C:3]#[CH:4]>CO.[Pd].CC([O-])=O.CC([O-])=O.[Pb+2]>[CH3:1][C:2]([CH3:29])([O:5][C:6]1[C:15]([O:16][C:17]([CH3:20])([CH3:21])[CH:18]=[CH2:19])=[C:14]2[C:9]([C:10](=[O:28])[CH:11]=[C:12]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[O:13]2)=[CH:8][CH:7]=1)[CH:3]=[CH2:4]

참가 물질

4

실험 절차

To a solution of 7,8-bis-(1,1-dimethyl-prop-2-ynyloxy)-2-phenyl-chromen-4-one (98 mg, 0.254 mmol) in methanol (20 mL) was added Lindlar's catalyst (Pd, 5 wt % on calcium carbonate, 25 mg) under argon. The mixture was stirred at room temperature for 50 min, then it was filtered through a syringe filter and the solvent was evaporated. The residue was purified by column chromatography (SiO2, EtOAc:hexanes/10-25%) to give the product as a white solid (72 mg, 73%): 1H NMR (CDCl3, 300 MHz) δ 7.98 (m, 2H), 7.81 (dd, J=0.9, 9.0 Hz, 1H), 7.52 (m, 3H), 7.16 (dd, J=0.6, 9.0 Hz, 1H), 6.75 (d, J=0.6 Hz, 1H), 6.22 (m, 2H), 5.24-5.12 (m, 3H), 4.98 (dd, J=1.2, 10.2 Hz, 1H), 1.56 (s, 6H), 1.55 (s, 6H); 13C NMR (CDCl3, 75 MHz) δ 178.1, 163.0, 154.9, 152.5, 136.0, 132.0, 131.2, 128.8, 126.6, 120.5, 119.6, 117.5, 107.3, 85.2, 74.9, 74.1, 73.9, 30.7, 29.8.

후처리

  1. filtrationit was filtered through a syringe
  2. filtrationfilter
  3. customthe solvent was evaporated
  4. customThe residue was purified by column chromatography (SiO2, EtOAc:hexanes/10-25%)

출처 및 근거

ORD 기록
ord-353bf79aa6cd4bdcaa923f586568c7ed
출처 데이터셋
uspto-grants-2009_09
특허 번호
US07592143B2

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