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Water → ({[2,2-Dimethoxy-1-(nitromethyl)ethyl]thio}methyl)benzene

HRID 504641
ノート
印刷プレビュー

反応式

HRID 504641 の反応式
[CH3:1][O:2][CH:3]([O:9][CH3:10])/[CH:4]=[CH:5]/[N+:6]([O-:8])=[O:7].[CH2:11]([SH:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.N1CCCCC1.O>C1(C)C=CC=CC=1>[CH3:1][O:2][CH:3]([O:9][CH3:10])[CH:4]([S:18][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:5][N+:6]([O-:8])=[O:7]
参加物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 962WaterHCID 7509Benzyl mercaptanHCID 8082PiperidineHCID 108772663,3-Dimethoxy-1-nitroprop-1-ene

生成物 1

HCID 59135946({[2,2-Dimethoxy-1-(nitromethyl)ethyl]thio}methyl)benzene収率 86%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A solution of (1E)-3,3-dimethoxy-1-nitroprop-1-ene (3.03 g, prepared according to Terahedron 2002, 58, 5773-5778), benzylmercaptan (2.54 ml) and piperidine (0.25 ml) in toluene (20 ml) was stirred at room temperature for 48 hr. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=0:100-20:80) to give the title compound (4.78 g, yield 86%) as a yellow oil.

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe extract was washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (ethyl acetate:hexane=0:100-20:80)

出典と根拠

ORDレコード
ord-1dabb2613dee46388eb1600da9b33331
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07777047B2

反応ノート

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