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4-Nitrobenzaldehyde → 4-[3-(4-Methylphenyl)-1-propenyl]nitrobenzene

HRID 1903655
ノート
印刷プレビュー

反応式

HRID 1903655 の反応式
[Br-].[CH3:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=[CH:5][CH:4]=1.C([Li])CCC.[N+:35]([C:38]1[CH:45]=[CH:44][C:41]([CH:42]=O)=[CH:40][CH:39]=1)([O-:37])=[O:36]>O1CCCC1.CCCCCC.O>[CH3:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH:10]=[CH:42][C:41]2[CH:44]=[CH:45][C:38]([N+:35]([O-:37])=[O:36])=[CH:39][CH:40]=2)=[CH:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 5414-NitrobenzaldehydeHCID 20466351(2-(P-Tolyl)ethyl)triphenylphosphonium bromideHCID 178418339Butyllithium

生成物 1

HCID 537641644-[3-(4-Methylphenyl)-1-propenyl]nitrobenzene収率 83%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 8028
Tetrahydrofuran
溶媒
2 回
HCID 8058Hexane溶媒

実験手順

To a suspension of [2-(4-methylphenyl)ethyl]triphenyl-phosphonium bromide (55.4 g) in anhydrous tetrahydrofuran (840 ml) kept at -50° C., a 1.5 N solution of n-butyl lithium in hexane (80 ml) was added, and the resultant mixture was stirred for a while. A solution of p-nitrobenzaldehyde (15.1 g) in anhydrous tetrahydrofuran (100 ml) was added thereto. The resulting mixture was allowed to stand at room temperature overnight, diluted with water and extracted with ethyl acetate. The extract was concentrated under reduced pressure and chromatographed on a column with silica gel, followed by eluting with a mixture of hexane and ethyl acetate to give 4-[3-(4-methylphenyl)-1-propenyl]nitrobenzene (21 g). nD24 1.5321.

後処理

  1. customkept at -50° C.
  2. extractionextracted with ethyl acetate
  3. concentrationThe extract was concentrated under reduced pressure
  4. customchromatographed on a column with silica gel
  5. washby eluting with a mixture of hexane and ethyl acetate

出典と根拠

ORDレコード
ord-9021908dc47c46efa83876e513d26111
出典データセット
uspto-grants-1984_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04437880

反応ノート

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