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Toluene → HCID 66724712、化合物

HRID 1027370
ノート
印刷プレビュー

反応式

HRID 1027370 の反応式
[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[CH2:6][CH:7]1[CH2:12][C:11](=[O:13])[CH2:10][C:9](=[O:14])[CH2:8]1.C(Cl)(Cl)Cl.C1(C)C=CC=CC=1.C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C.[Cl:38][C:39]1[CH:44]=[CH:43][C:42]([C:45]2[CH:50]=[CH:49][C:48]([CH3:51])=[C:47]([Pb+3])[CH:46]=2)=[CH:41][CH:40]=1>ClCCl>[Cl:38][C:39]1[CH:40]=[CH:41][C:42]([C:45]2[CH:50]=[CH:49][C:48]([CH3:51])=[C:47]([CH:10]3[C:11](=[O:13])[CH2:12][CH:7]([CH2:6][CH:2]4[O:3][CH2:4][CH2:5][O:1]4)[CH2:8][C:9]3=[O:14])[CH:46]=2)=[CH:43][CH:44]=1
参加物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 1140TolueneHCID 6212ChloroformHCID 58079363HCID 58079363、化合物HCID 178476525HCID 178476525、化合物

生成物 1

HCID 66724712HCID 66724712、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 5-[1,3]dioxolan-2-ylmethylcyclohexane-1,3-dione (1.43 g, 7.22 mmol) in a mixed solvent system of chloroform (72 ml) and toluene (18 ml) is added N,N-dimethylaminopyridine (4.40 g, 36.08 mmol) and the solution is stirred at room temperature for 10 minutes. To this mixture is then added 4′-chloro-4-methylbiphenyl-3-yllead triacetate (described in WO 2008/071405) (4.95 g, 7.91 mmol) in one portion, followed by heating at 80° C. for 2 hours. After cooling to room temperature the solution is diluted with dichloromethane (90 ml) and quenched with 1M hydrochloric acid (90 ml). The resulting precipitate is filtered through celite and the residue washed with additional dichloromethane (20 ml). The biphasic solution is separated and the organic layer further washed with 1M hydrochloric acid (45 ml). Organics are finally passed through a phase separator then concentrated in vacuo to afford the crude product as a yellow oil. After flash column chromatography on silica (7:1 ethyl acetate/hexane eluant) 2-(4′-chloro-4-methylbiphenyl-3-yl)-5-[1,3]dioxolan-2-ylmethylcyclohexane-1,3-dione is afforded as a cream solid.

後処理

  1. temperatureby heating at 80° C. for 2 hours
  2. temperatureAfter cooling to room temperature the solution
  3. customquenched with 1M hydrochloric acid (90 ml)
  4. filtrationThe resulting precipitate is filtered through celite
  5. washthe residue washed with additional dichloromethane (20 ml)
  6. customThe biphasic solution is separated
  7. washthe organic layer further washed with 1M hydrochloric acid (45 ml)
  8. concentrationthen concentrated in vacuo
  9. customto afford the crude product as a yellow oil

出典と根拠

ORDレコード
ord-3330adb34ddb443dba77fde47d450a96
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08735322B2

反応ノート

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