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Allyl bromide → Ethyl 7-allyloxynaphthalene-2-carboxylate

HRID 463328
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HRID 463328 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

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

생성물 1

HCID 20282953Ethyl 7-allyloxynaphthalene-2-carboxylate수율 81%

시약·촉매·용매 2

HCID 4875Potassium Iodide촉매HCID 180Acetone
용매

실험 절차

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°.

후처리

  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)

출처 및 근거

ORD 기록
ord-010ec888aa54404db7f6eec6f76e531c
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04518612

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