Bromine → 1,1,3,4,4,6-Hexamethyl-7-bromacetyl-1,2,3,4-tetrahydronaphthalene

HRID 1414452

反応式

HRID 1414452 の反応式
[CH3:1][C:2]1([CH3:19])[C:11]2[C:6](=[CH:7][C:8]([CH3:15])=[C:9]([C:12](=[O:14])[CH3:13])[CH:10]=2)[C:5]([CH3:17])([CH3:16])[CH:4]([CH3:18])[CH2:3]1.[Br:20]Br>C(O)(=O)C>[CH3:1][C:2]1([CH3:19])[C:11]2[C:6](=[CH:7][C:8]([CH3:15])=[C:9]([C:12](=[O:14])[CH2:13][Br:20])[CH:10]=2)[C:5]([CH3:17])([CH3:16])[CH:4]([CH3:18])[CH2:3]1

参加物

4

反応物 2

HCID 24408BromineHCID 89440Tonalide

生成物 1

HCID 214306251,1,3,4,4,6-Hexamethyl-7-bromacetyl-1,2,3,4-tetrahydronaphthalene収率 38%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

1,1,3,4,4,6-Hexamethyl-7-acetyl-1,2,3,4-tetrahydronaphthalene (33 gm,0.12 m) was dissolved in glacial acetic acid (40 ml.) and the solution treated portionwise with bromine (20.3 gm) with stirring. The mixture was allowed to stand overnight at room temperature and poured onto ice (100 gm.). The resulting mixture was extracted with ether (3 ×100 ml.) and the combined extracts washed with saturated sodium carbonate (2 × 50 ml.) and then brine. The washed extracts were then dried (MgSO4) and the solvent removed in vacuo to give a crystalline solid. This was recrystallised from absolute ethanol to give 1,1,3,4,4,6-hexamethyl-7-bromoacetyl-1,2,3,4-tetrahydronaphthalene as colourless needles (16 gm, 38%) m.p. 68°C. [Found: C, 64.40; H, 7.65%. C18H25BrO requires: C,64.09; H,7.47%].

後処理

  1. additionpoured onto ice (100 gm.)
  2. extractionThe resulting mixture was extracted with ether (3 ×100 ml.)
  3. washthe combined extracts washed with saturated sodium carbonate (2 × 50 ml.)
  4. dry with materialThe washed extracts were then dried (MgSO4)
  5. customthe solvent removed in vacuo
  6. customto give a crystalline solid
  7. customThis was recrystallised from absolute ethanol

出典と根拠

ORDレコード
ord-712eb967d0094554b638fc008943ee9b
出典データセット
uspto-grants-1977_01
特許番号
US04001330

関連ノート

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