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Sodium Nitrite → HCID 178472910、化合物

HRID 324424
ノート
印刷プレビュー

反応式

HRID 324424 の反応式
[N:1]([O-:3])=O.[Na+].[CH3:5][C:6]1[CH:7]=[C:8]([CH2:12][CH2:13][C:14](=[O:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH:9]=[CH:10][CH:11]=1>O.C(O)(=O)C>[OH:3][N:1]=[C:15]([C:14](=[O:21])[CH2:13][CH2:12][C:8]1[CH:9]=[CH:10][CH:11]=[C:6]([CH3:5])[CH:7]=1)[C:16]([O:18][CH2:19][CH3:20])=[O:17]
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 23668193Sodium NitriteHCID 54309110Ethyl 3-oxo-5-m-toluylpentanoate

生成物 1

HCID 178472910HCID 178472910、化合物

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 962Water溶媒2 回

実験手順

Sodium nitrite (32 g) in water (60 ml) was added dropwise over 1 hour to a stirred solution of the product from example 13 step (i) (99.4 g) in acetic acid (200 ml) at a rate such that the internal temperature did not rise above 30° C. The solution was allowed to stir a further 1 hour before adding water (500 ml). After stirring for a further 24 h the reaction mixture was extracted with diethyl ether (×4). The combined ether extracts were washed with saturated sodium bicarbonate solution, and finally water before collecting the organic layer and drying over magnesium sulphate. The solution was filtered and the solvent evaporated under reduced pressure to leave the subtitle product.

後処理

  1. customdid not rise above 30° C
  2. stirringAfter stirring for a further 24 h the reaction mixture
  3. extractionwas extracted with diethyl ether (×4)
  4. washThe combined ether extracts were washed with saturated sodium bicarbonate solution, and finally water
  5. custombefore collecting the organic layer
  6. dry with materialdrying over magnesium sulphate
  7. filtrationThe solution was filtered
  8. customthe solvent evaporated under reduced pressure

出典と根拠

ORDレコード
ord-9cf04f13af854fc48aded8d0d453957a
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06218376B1

反応ノート

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