Sodium Carbonate → 2-(2-Furyl)-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan

HRID 2059636노트

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HRID 2059636 반응식
I[C:2]1([O:9][CH3:10])[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][CH2:3]1.[O:11]1[CH:15]=[CH:14][CH:13]=[C:12]1[C:16]#[C:17][C:18]([C:20]1[CH:25]=[C:24]([O:26][CH3:27])[C:23]([O:28][CH3:29])=[C:22]([O:30][CH3:31])[CH:21]=1)=[O:19].[Li+].[Cl-].C([O-])([O-])=O.[Na+].[Na+]>CN(C=O)C>[O:11]1[CH:15]=[CH:14][CH:13]=[C:12]1[C:16]1[O:8][C:6]2[CH:7]=[C:2]([O:9][CH3:10])[CH:3]=[CH:4][C:5]=2[C:17]=1[C:18](=[O:19])[C:20]1[CH:25]=[C:24]([O:26][CH3:27])[C:23]([O:28][CH3:29])=[C:22]([O:30][CH3:31])[CH:21]=1

참가 물질

6

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온도
102.5 °C

실험 절차

5-Iodo-5-methoxyphenol (125 mg, 0.5 mmol), 3-(2-furyl)-1-(3,4,5-trimethoxyphenyl)-prop-2-yn-1-one (172 mg, 0.6 mmol), LiCl (21.2 mg, 0.5 mmol) and Na2CO3 (265 mg, 2.5 mmol) were added to anhydrous DMF (3 ml) and flushed with N2 three times. Pd(OAc)2 was added to the reaction mixture and again flushed with N2. The reaction mixture was heated to 100-105° C. for 6 h and then reaction was cooled to room temp. Quenched by addition of aqueous NH4Cl solution and extracted with EtOAc. 2-(2-Furyl)-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan was isolated in 12% yield by silica gel column chromatography using 20 to 40% EtOAc in hexane. 1H NMR (300 MHz, CDCl3) δ: 3.75(s, 6H, OMe), 3.86(s, 3H, OMe), 3.90(s, 3H, OMe), 6.44-6.46(m, 1H), 6.87(dd, J=2.1, 8.7, 1H), 6.97(d, J=3.6, 1H), 7.07(d, J=2.1, 1H), 7.15(s, 2H), 7.36(d, J=8.7, 1H), 7.41(d, J=1.2, 1H). MS (ES) m/z: 408.9(M+H)+.

후처리

  1. customflushed with N2 three times
  2. additionPd(OAc)2 was added to the reaction mixture
  3. customagain flushed with N2
  4. customreaction
  5. temperaturewas cooled to room temp
  6. customQuenched by addition of aqueous NH4Cl solution
  7. extractionextracted with EtOAc

출처 및 근거

ORD 기록
ord-3d2bc53a70ff47aaad9791e50b3ebc3d
출처 데이터셋
uspto-grants-2012_10
특허 번호
US08278290B2

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