Dimethyl Sulfoxide → Benzyl 6-oxohexylcarbamate

HRID 376106

反応式

HRID 376106 の反応式
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH2:11]([O:18][C:19]([NH:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][OH:28])=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(N(C(C)C)C(C)C)C>C(Cl)Cl>[CH2:11]([O:18][C:19]([NH:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH:27]=[O:28])=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

参加物

6

実験手順

0.32 ml (4.40 mmol) of dimethyl sulfoxide is added dropwise under nitrogen to a solution of 0.19 ml (2.20 mmol) of oxalyl chloride in 10 ml of methylene chloride which is being stirred at -50°. The mixture is stirred for 15 minutes, and then 0.5 g (2 mmol) of 6-(N-benzyloxycarbonylamino)hexan-1-ol is added. Stirring is continued at -50° for 25 minutes, 1.78 ml (10 mmol) of N-ethyl-N,N-diisopropylamine are added dropwise and the mixture is poured into 10 ml of ice-water. The organic phase is separated off and the aqueous phase is extracted with 10 ml of methylene chloride. The organic phases are combined, washed twice with 5 ml of N-hydrochloric acid each time and once with 10 ml of saturated sodium chloride solution, dried over magnesium sulfate and concentrated to dryness by evaporation. The resulting oil is purified by chromatography on silica gel with hexane/ethyl acetate (1:1) as eluant. 6-(N-benzyloxycarbonylamino)hexanal is obtained.

後処理

  1. stirringThe mixture is stirred for 15 minutes
  2. stirringStirring
  3. customThe organic phase is separated off
  4. extractionthe aqueous phase is extracted with 10 ml of methylene chloride
  5. washwashed twice with 5 ml of N-hydrochloric acid each time
  6. dry with materialonce with 10 ml of saturated sodium chloride solution, dried over magnesium sulfate
  7. concentrationconcentrated to dryness by evaporation
  8. customThe resulting oil is purified by chromatography on silica gel with hexane/ethyl acetate (1:1) as eluant

出典と根拠

ORDレコード
ord-755e5197606248ab8d01e0d53922ddc1
出典データセット
uspto-grants-1996_01
特許番号
US05488140

関連ノート

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