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Potassium Carbonate → HCID 23437305, 화합물

HRID 2120019
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HRID 2120019 반응식
[OH:1][C:2]1[C:19]([O:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])=[CH:18][C:17]2[C:16]3[C:11](=[CH:12][C:13]([O:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40])=[C:14]([O:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[CH:15]=3)[C:10]3[C:5](=[CH:6][C:7]([O:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH3:54])=[C:8]([O:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH3:47])[CH:9]=3)[C:4]=2[CH:3]=1.Br[CH2:56][CH2:57][O:58][CH2:59][CH2:60][O:61][CH3:62].C(=O)([O-])[O-].[K+].[K+]>C(O)C>[O:1]([C:2]1[C:19]([O:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])=[CH:18][C:17]2[C:16]3[C:11](=[CH:12][C:13]([O:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40])=[C:14]([O:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[CH:15]=3)[C:10]3[C:5](=[CH:6][C:7]([O:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH3:54])=[C:8]([O:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH3:47])[CH:9]=3)[C:4]=2[CH:3]=1)[CH2:56][CH2:57][O:58][CH2:59][CH2:60][O:61][CH3:62]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 1235321-Bromo-3,6-dioxaheptaneHCID 15399808HCID 15399808, 화합물

생성물 1

HCID 23437305HCID 23437305, 화합물수율 14.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 2-hydroxy-3,6,7,10,11-pentahexyloxytriphenylene (0.37 g, 0.5 mmol), 1-bromo-2-(2-methoxyethoxy)ethane (0.37 g) and potassium carbonate (0.4 g, 3 mmol) in ethanol (10 ml) was heated under reflux for 72 hours. After which time, it was filtered, extracted with dichloromethane (25 ml), concentrated in vacuo, and the product isolated by column chromatography (silica gel eluting with ethyl acetate) and recrystallised from ethanol to give the title compound as a white solid (0.06 g, 14%, K→D 55.4° C., D→I 69.3° C.). Elemental Analysis: C, 74.95; H, 9.55. C53H82O8 requires: C, 75.14; H, 9.75. Mass Spectrum: m/z (FAB) 869 ([M+23]+, 100%); 846 (M+, 94.5%). 1H-NMR: δH (CDCl3) 0.93 (15H, t, J=6.7 Hz, O(CH2)5CH3), 1.10-1.70 (30H, m, OCH2CH2(CH2)3), 1.94 (10H, m, OCH2CH2), 3.41 (3H, s, OCH2CH2OCH2CH2CH3), 3.61 (2H, t, J=5.0 Hz, OCH2CH2OCH2CH2), 3.82 (2H, t, J=5.0 Hz, OCH2CH2OCH2), 4.00 (2H, t, J=5.0 Hz, OCH2CH2), 4.23 (10H, t, J=6.5 Hz, OCH2), 4.42 (2H, t, J=5.0 Hz, OCH2), 7.83 (5H, s, ArH), 7.90 (1H, s, ArH).

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 72 hours
  3. filtrationAfter which time, it was filtered
  4. extractionextracted with dichloromethane (25 ml)
  5. concentrationconcentrated in vacuo
  6. customthe product isolated by column chromatography (silica gel eluting with ethyl acetate)
  7. customrecrystallised from ethanol

출처 및 근거

ORD 기록
ord-18f76a9336f14e0fb23a0eb449120073
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06689290B2

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