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Allyl bromide → Ethyl 7-allyloxynaphthalene-2-carboxylate

HRID 463328
ノート
印刷プレビュー

反応式

HRID 463328 の反応式
[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:9]2)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:23](Br)[CH:24]=[CH2:25]>[I-].[K+].CC(C)=O>[CH2:25]([O:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:9]2)=[CH:4][CH:3]=1)[CH:24]=[CH2:23]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 7841Allyl bromideHCID 11430Potassium CarbonateHCID 12635629Ethyl 7-hydroxynaphthalene-2-carboxylate

生成物 1

HCID 20282953Ethyl 7-allyloxynaphthalene-2-carboxylate収率 81%

試薬・触媒・溶媒 2

HCID 4875Potassium Iodide触媒HCID 180Acetone
溶媒

実験手順

A mixture of ethyl 7-hydroxynaphthalene-2-carboxylate (37.5 g), anhydrous potassium carbonate (24.0 g), potassium iodide (0.5 g), and allyl bromide (29.0 g) was heated in refluxing acetone (200 ml) with stirring for 15 hours. The mixture was filtered and the filtrate was evaporated. The residue was dissolved in ethyl-acetate, washed with 2% sodium hydroxide solution and water, dried and evaporated to give a solid. Crystallisation from petroleum ether (b.p. 40-60) afforded ethyl 7-allyloxynaphthalene-2-carboxylate (36 g), m.p. 60°-61°.

後処理

  1. temperaturewas heated
  2. filtrationThe mixture was filtered
  3. customthe filtrate was evaporated
  4. dissolutionThe residue was dissolved in ethyl-acetate
  5. washwashed with 2% sodium hydroxide solution and water
  6. customdried
  7. customevaporated
  8. customto give a solid
  9. customCrystallisation from petroleum ether (b.p. 40-60)

出典と根拠

ORDレコード
ord-010ec888aa54404db7f6eec6f76e531c
出典データセット
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04518612

反応ノート

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