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Dimethyl Sulfoxide → HCID 54105440、化合物

HRID 2396480
ノート
印刷プレビュー

反応式

HRID 2396480 の反応式
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH3:11][C@@:12]([OH:19])([C:15]([CH3:18])([CH3:17])[CH3:16])[CH2:13][OH:14].C(N(CC)CC)C>C(Cl)Cl>[CH3:11][C@@:12]([OH:19])([C:15]([CH3:18])([CH3:17])[CH3:16])[CH:13]=[O:14]
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 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 24741476(2R)-2,3,3-Trimethylbutane-1,2-diol

生成物 1

HCID 54105440HCID 54105440、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒3 回

反応条件

温度
-78 °C

実験手順

A solution of dimethylsulfoxide (2,578 ml. 36.3 mmol) in methylene chloride (3 ml) was added dropwise at -78° C. to a stirred solution of oxalyl chloride (1.585 ml, 18.2 mmol) over 5 minutes and stirred at -78° C. for 10 minutes. A solution of (R)-2,3,3-trimethyl-1,2-butanediol in methylene chloride (25 ml) was added dropwise and stirred for 15 minutes at -78° C. Triethylamine (11.51 ml, 82.6 mmol) was added and the reaction was allowed to come to room temperature. The mixture was diluted with additional methylene chloride, washed with 10% sulfuric acid, the combined aqueous phase was extracted with methylene chloride, and the combined organic layer was washed with saturated sodium bicarbonate, dried (magnesium sulfate), and concentrated by distillation at atmospheric pressure to afford 2.15 g of (R)-2,3,3-trimethyl-2-hydroxybutanal as a pale gummy solid.

後処理

  1. stirringstirred for 15 minutes at -78° C
  2. customto come to room temperature
  3. washwashed with 10% sulfuric acid
  4. extractionthe combined aqueous phase was extracted with methylene chloride
  5. washthe combined organic layer was washed with saturated sodium bicarbonate
  6. dry with materialdried (magnesium sulfate)
  7. concentrationconcentrated by distillation at atmospheric pressure

出典と根拠

ORDレコード
ord-45527cfe074a4fdf8a48ae0a83b0e501
出典データセット
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05492910

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート