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Ethanol, reaction products with ammonia, distn. residues → (E)-1-(2-Aminoethylidene)-6-methoxyindan

HRID 1977991
ノート
印刷プレビュー

反応式

HRID 1977991 の反応式
[CH3:1][O:2][C:3]1[CH:11]=[C:10]2[C:6]([CH2:7][CH2:8][C:9]2=[CH:12][C:13]#[N:14])=[CH:5][CH:4]=1.N.C(O)C>C(O)C.[Co]>[NH2:14][CH2:13]/[CH:12]=[C:9]1\[CH2:8][CH2:7][C:6]2[C:10]\1=[CH:11][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 22020343Ethanol, reaction products with ammonia, distn. residuesHCID 53954914(6-Methoxyindan-1-ylidene) acetonitrile

生成物 1

HCID 10987044(E)-1-(2-Aminoethylidene)-6-methoxyindan収率 86%

試薬・触媒・溶媒 2

HCID 104730Cobalt触媒HCID 702Ethanol溶媒

実験手順

To a solution of (6-methoxyindan-1-ylidene) acetonitrile (1.60 g, 8.64 mmol) in ethanol (80 ml) were added a 2M ammonia/ethanol solution (40 ml) and Raney cobalt (1.6 g). The mixture was stirred, under hydrogen atmosphere (4 kgf/cm2), for 32 hours at 40° C., and for further 8 hours at 70° C. The Raney cobalt was filtered off, then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (chloroform:methanol=9:1 to chloroform:methanol:triethylamine=90:8:2) to give the above-titled compound (yield 1.40 g, 86%, oily).

後処理

  1. waitfor further 8 hours at 70° C
  2. filtrationThe Raney cobalt was filtered off
  3. distillationthe solvent was distilled off under reduced pressure
  4. customThe residue was purified by means of a silica gel column chromatography (chloroform:methanol=9:1 to chloroform:methanol:triethylamine=90:8:2)

出典と根拠

ORDレコード
ord-34cb841497864788b307d63b51f391d7
出典データセット
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06235789B1

反応ノート

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