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Sulfuric Acid → 3,7-Dimethylocta-2,6-Dienal

HRID 1252789
ノート
印刷プレビュー

反応式

HRID 1252789 の反応式
[CH2:1](Cl)/[CH:2]=[C:3](/[CH2:5][CH2:6][CH:7]=[C:8]([CH3:10])[CH3:9])\[CH3:4].C([N+]1([O-])CC[O:17]CC1)C.CN(C)C=O.S(=O)(=O)(O)O>C(OCC)(=O)C>[CH3:9][C:8](=[CH:7][CH2:6][CH2:5][C:3](=[CH:2][CH:1]=[O:17])[CH3:4])[CH3:10]
参加物反応条件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 1118Sulfuric AcidHCID 6228DimethylformamideHCID 759864-Ethylmorpholine 4-oxideHCID 6372219Geranyl chloride

生成物 1

HCID 88433,7-Dimethylocta-2,6-Dienal収率 88%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

反応条件

温度
50 °C

実験手順

346 mg (2 mmols) of geranyl chloride and 787 mg (6 mmols) of N-ethylmorpholine N-oxide were placed in a flask, to which was further added 3 ml of N,N-dimethylformamide. The mixture was agitated at room temperature for 1 hour and at 50° C. for 4 hours. To the reaction mixture was added 10 ml of 2.5% sulfuric acid and 10 ml of ethyl acetate for phase separation. The resultant organic phase was washed with 5 ml of 2.5% sulfuric acid, 5 ml of a saturated sodium hydrogen carbonate aqueous solution and 5 ml of a 10% sodium sulfate aqueous solution successively, after which it was dried with magnesium sulfate. After the drying, the solvent was distilled off from the solution and the residue was subjected to distillation by the use of Kugel-rohr distillation apparatus (bath temperature 93° C./3 Torr.) to obtain 268 mg (1.76 mmols) of citral. The yield was 88%.

後処理

  1. customfor phase separation
  2. washThe resultant organic phase was washed with 5 ml of 2.5% sulfuric acid, 5 ml of a saturated sodium hydrogen carbonate aqueous solution and 5 ml of a 10% sodium sulfate aqueous solution successively
  3. dry with materialafter which it was dried with magnesium sulfate
  4. distillationAfter the drying, the solvent was distilled off from the solution
  5. distillationthe residue was subjected to distillation by the use of Kugel-rohr distillation apparatus (bath temperature 93° C./3 Torr.)

出典と根拠

ORDレコード
ord-737cf806fb344cfc962b805f11395ba3
出典データセット
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04745229

反応ノート

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