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Triethylamine → cis 2-(3,4,5-Trimethoxyphenyl)-5-(3-phthalimidyl propoxy) tetrahydrofuran

HRID 1490245
ノート
印刷プレビュー

反応式

HRID 1490245 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:13]2[CH2:17][CH2:16][CH:15]([OH:18])[O:14]2)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].C(N(CC)CC)C.FC(F)(F)C(OC(=O)C(F)(F)F)=O.[C:39]1(=[O:53])[N:43]([CH2:44][CH2:45][CH2:46]O)[C:42](=[O:48])[C:41]2=[CH:49][CH:50]=[CH:51][CH:52]=[C:40]12>ClCCl>[CH3:12][O:11][C:7]1[CH:6]=[C:5]([C@H:13]2[CH2:17][CH2:16][C@@H:15]([O:18][CH2:46][CH2:45][CH2:44][N:43]3[C:39](=[O:53])[C:40]4=[CH:52][CH:51]=[CH:50][CH:49]=[C:41]4[C:42]3=[O:48])[O:14]2)[CH:4]=[C:3]([O:2][CH3:1])[C:8]=1[O:9][CH3:10]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8471TriethylamineHCID 9845Trifluoroacetic anhydrideHCID 701602-(3-Hydroxypropyl)isoindoline-1,3-dioneHCID 190650382-(3,4,5-Trimethoxyphenyl)-5-hydroxy-tetrahydrofuran

生成物 1

HCID 86751456cis 2-(3,4,5-Trimethoxyphenyl)-5-(3-phthalimidyl propoxy) tetrahydrofuran収率 46%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

反応条件

温度
0 °C

実験手順

Compound 105 (1.14 g, 4.49 mmol) was dissolved in 4 mL dichloromethane. Triethylamine (681.4 mg, 6.73 mmol) was added to this solution. The reaction mixture was cooled with an ice bath and trifluoroacetic anhydride (1.41 g, 6.73 mmol) was added in a dropwise manner. The reaction mixture was stirred at 0° C. for 30 minutes and then 3-phthalimidylpropanol (106) (2.4 g, 13.26 mmol) was added. The reaction mixture was warmed to room temperature and stirred at room temperature for 2 hours. The reaction was quenched with saturated aqueous NaHCO3 solution and extracted with ethyl acetate. The organic layer was washed with water and saturated NaCl solution, dried over MgSO4, filtered and evaporated in vacuo to an oil which was purified by column chromatography (silica, 2:1 hexane/ethyl acetate) (107: 522 mg (trans); 108: 271 mg (cis); 1:1 mixture of 107 and 108: 110 mg; total yield 46%) . 1H NMR (CDCl3): 107: 1.70 (m,1H); 1.82 (m,1H); 2.00(m,2H); 2.02(m,1H); 2.28(m,1H); 3.46(m,1H); 3.83(s,3H); 3.84(m,3H); 3.88(s,6H); 4.99(t,1H); 5.30(dd,1H); 6.56(s,2H); 7.72(m,2H); 7.85(m,2H). 108: 1.95(m,3H); 2.00(m,2H); 2.20(m,1H); 3.51(m,1H); 3.83(s,3H); 3.85(m,2H); 3.88(s,6H); 3.92(m,1H); 4.90(m,1H); 5.16(dd,1H); 6.60(s,2H); 7.72(m,2H); 7.84(m,2H).

後処理

  1. temperatureThe reaction mixture was cooled with an ice bath
  2. temperatureThe reaction mixture was warmed to room temperature
  3. stirringstirred at room temperature for 2 hours
  4. customThe reaction was quenched with saturated aqueous NaHCO3 solution
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with water and saturated NaCl solution
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. customevaporated in vacuo to an oil which
  10. customwas purified by column chromatography (silica, 2:1 hexane/ethyl acetate) (107: 522 mg (trans); 108: 271 mg (cis); 1:1 mixture of 107 and 108: 110 mg; total yield 46%)

出典と根拠

ORDレコード
ord-fe73c643d9524284b633570bbae68428
出典データセット
uspto-grants-1997_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05681966

反応ノート

読み込み中…

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