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Dimethyl Sulfoxide → HCID 54105440, 화합물

HRID 2396480
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HRID 2396480 반응식
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]
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6

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HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 24741476(2R)-2,3,3-Trimethylbutane-1,2-diol

생성물 1

HCID 54105440HCID 54105440, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

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온도
-78 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-45527cfe074a4fdf8a48ae0a83b0e501
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05492910

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