Methanol → 11,11-Diphenyl-11-methoxyundec-1-ene

HRID 275465ノート

反応式

HRID 275465 の反応式
[H-].[Na+].CO.[C:5]1([C:11]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)([OH:22])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH:20]=[CH2:21])[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[CH3:29]OS(OC)(=O)=O>C1COCC1>[C:23]1([C:11]([C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=2)([O:22][CH3:29])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH:20]=[CH2:21])[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1

参加物

6

反応物 4

HCID 887Methanol2 回HCID 6497Dimethyl SulfateHCID 24758Sodium hydrideHCID 200883261,1-Diphenyl-10-undecen-1-ol

生成物 1

HCID 2008832511,11-Diphenyl-11-methoxyundec-1-ene

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a mixture of 1.2 g of sodium hydride and 0.1 mL of methanol in 50 mL of THF was added a solution of 10 g of 1,1-diphenyl-10-undecen-1-ol in 20 mL of THF over 2 hrs. The mixture was stirred at room temperature for 4 hrs, then 3.5 mL of dimethylsulfate was added. The mixture was stirred for an additional 75 hrs, then 2 mL of methanol was added to quench any excess sodium hydride. The solvent was distilled in vacuo, the residue taken up in ether, and the solution washed with 10% by wt of hydrochloric acid, water, and saturated sodium hydrogen carbonate. The solution was then dried with sodium sulfate and concentrated in vacuo to give 10.6 g of 11,11-diphenyl-11-methoxyundec-1-ene which is characterized by:

後処理

  1. stirringThe mixture was stirred for an additional 75 hrs
  2. customto quench any excess sodium hydride
  3. distillationThe solvent was distilled in vacuo
  4. washthe solution washed with 10% by wt of hydrochloric acid, water, and saturated sodium hydrogen carbonate
  5. dry with materialThe solution was then dried with sodium sulfate
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-aacae9c137504bb6b2733f63487142c0
出典データセット
uspto-grants-1995_02
特許番号
US05393795

反応ノート

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