Dimethyl Sulfoxide → 79091-88-6

HRID 1961630ノート

反応式

HRID 1961630 の反応式
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH3:11][O:12][C:13]([C@@H:15]1[CH2:18][CH2:17][C@H:16]1[CH2:19][OH:20])=[O:14].C(N(CC)CC)C>ClCCl.O>[CH3:11][O:12][C:13]([C@@H:15]1[CH2:18][CH2:17][C@H:16]1[CH:19]=[O:20])=[O:14]

参加物

7

反応条件

温度
-78 °C

実験手順

At −78° C., oxalyl Chloride (9.2 mL, 106.5 mmol) was solved in dichloromethane (250 mL) and (15.5 mL, 218 mmol) of dimethylsulfoxide in 20 mL of dichloromethane was added. After 15 minutes of stirring at −78° C., Trans-2-Hydroxymethyl-cyclobutanecarboxylic acid methyl ester (14 g, 95.17 mmol) was added in 78 mL of dichloromethane and 10 minutes later triethylamine (67 mL, 479 mmol) was added and the mixture was stirred for 2 h at −78° C. 150 mL of dichloromethane added and 200 mL of water were added and the aqueous phase was extracted with 200 mL of dichlormethane and the combined organic phases were purified with column chromatography on silica using n-heptane/AcOEt (4+1) to yield 11.1 g, (78 mmol, 82% yield) of the title compound as a colourless liquid. MS (m/e): 165.2 (M+Na+)

後処理

  1. customAt −78° C.
  2. additionwas added
  3. stirringthe mixture was stirred for 2 h at −78° C
  4. extractionthe aqueous phase was extracted with 200 mL of dichlormethane
  5. customthe combined organic phases were purified with column chromatography on silica

出典と根拠

ORDレコード
ord-0e08f3f471be4f8baa266dc43455543b
出典データセット
uspto-grants-2013_04
特許番号
US08415350B2

反応ノート

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