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N,N,N',N'-Tetramethylethylenediamine → 1-[2,5-Dimethoxy-3,6-bis(methoxymethoxy)phenyl]5-[2,5-dimethoxy-3,6-bis(methoxymethoxy)-4-(methylthio)phenyl]pentane

HRID 1588166
ノート
印刷プレビュー

反応式

HRID 1588166 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH2:10][O:11][CH3:12])[C:6]([O:13][CH3:14])=[C:5]([S:15][CH3:16])[C:4]=1[O:17][CH2:18][O:19][CH3:20].CN(C)CCN(C)C.C([Li])CCC.I[CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][C:40]1[C:45]([O:46][CH2:47][O:48][CH3:49])=[C:44]([O:50][CH3:51])[CH:43]=[C:42]([O:52][CH2:53][O:54][CH3:55])[C:41]=1[O:56][CH3:57]>C1(C)C=CC=CC=1.CN(C)P(=O)(N(C)C)N(C)C.C(OCC)C>[CH3:57][O:56][C:41]1[C:42]([O:52][CH2:53][O:54][CH3:55])=[CH:43][C:44]([O:50][CH3:51])=[C:45]([O:46][CH2:47][O:48][CH3:49])[C:40]=1[CH2:39][CH2:38][CH2:37][CH2:36][CH2:35][C:8]1[C:7]([O:9][CH2:10][O:11][CH3:12])=[C:6]([O:13][CH3:14])[C:5]([S:15][CH3:16])=[C:4]([O:17][CH2:18][O:19][CH3:20])[C:3]=1[O:2][CH3:1]
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

8

反応物 4

HCID 8037N,N,N',N'-TetramethylethylenediamineHCID 197571571,4-Dimethoxy-2,5-bis(methoxymethoxy)-3-methylthiobenzeneHCID 197572171-(5-Iodopent-1-yl)-2,5-dimethoxy-3,6-bis(methoxymethoxy)benzeneHCID 178418339Butyllithium

生成物 1

HCID 197572321-[2,5-Dimethoxy-3,6-bis(methoxymethoxy)phenyl]5-[2,5-dimethoxy-3,6-bis(methoxymethoxy)-4-(methylthio)phenyl]pentane

試薬・触媒・溶媒 3

HCID 1140Toluene溶媒2 回HCID 3283Diethyl Ether溶媒HCID 12679Hexamethylphosphoramide溶媒

反応条件

温度
-78 °C

実験手順

150 Milligrams of 1,4-dimethoxy-2,5-bis(methoxymethoxy)-3-(methylthio)benzene was dissolved in a mixed solvent of 4 ml of toluene with 1 ml of hexamethylphosphoric triamide, to this solution was added 0.104 ml of N,N,N',N'-tetramethylethylenediamine was added, then the whole mixture was cooled to -78° C. on a dry ice-acetone bath. 0.466 Milliliter of n-butyllithium (1.6 M, n-hexane solution) was added dropwise thereto and stirred for 30 minutes. Next, 8 ml of toluene solution containing 269 mg of 1-(5-iodopent-1-yl)-2,5-dimethoxy-3,6-bis(methoxymethoxy)benzene was added dropwise and the reaction mixture was stirred overnight. The reaction mixture was warmed to room temperature, then 30 ml of diethyl ether was added thereto, the organic layer was washed three times with 20 ml of water then washed twice with a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. The diethyl ether solution was concentrated under reduced pressure, the residue obtained was purified by means of a preparative thin layer chromatography (thickness: 2 mm, adsorbent: Merck Art 5717 silica gel, developing solvent: 40% ethyl acetate-n-hexane). There was obtained 120 mg of 1-[2,5-dimethoxy3,6-bis(methoxymethoxy)phenyl]-5-[2,5-dimethoxy-3,6-bis(methoxymethoxy)-4-(methylthio)phenyl]pentane as in the form of colorless oily substance.

後処理

  1. additionwas added
  2. additionwas added dropwise
  3. stirringthe reaction mixture was stirred overnight
  4. temperatureThe reaction mixture was warmed to room temperature
  5. washthe organic layer was washed three times with 20 ml of water
  6. washthen washed twice with a saturated sodium chloride aqueous solution
  7. dry with materialdried over anhydrous magnesium sulfate
  8. concentrationThe diethyl ether solution was concentrated under reduced pressure
  9. customthe residue obtained
  10. customwas purified by means of a preparative thin layer chromatography (thickness: 2 mm, adsorbent: Merck Art 5717 silica gel, developing solvent: 40% ethyl acetate-n-hexane)

出典と根拠

ORDレコード
ord-26ee9881982c4b0785e21e3db592d884
出典データセット
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05220042

反応ノート

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