Hydrochloric Acid → 4-Cyclopentyloxy-3-hydroxybenzaldehyde

HRID 131587

반응식

HRID 131587 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[OH:10])[CH:5]=[O:6].C(=O)([O-])[O-].[K+].[K+].[CH:17]1(Br)[CH2:21][CH2:20][CH2:19][CH2:18]1.Cl>CN(C=O)C.O>[CH:17]1([O:10][C:9]2[CH:8]=[CH:7][C:4]([CH:5]=[O:6])=[CH:3][C:2]=2[OH:1])[CH2:21][CH2:20][CH2:19][CH2:18]1

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 8728BromocyclopentaneHCID 87683,4-DihydroxybenzaldehydeHCID 11430Potassium Carbonate

생성물 1

HCID 167261494-Cyclopentyloxy-3-hydroxybenzaldehyde수율 67%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

A suspension of 3,4-dihydroxybenzaldehyde (5.0 gm, 0.0362 mol), anhydrous potassium carbonate (6.0 gm, 0.0434 mol) and cyclopentyl bromide (6.5 gm, 0.0434 mol) in dry DMF (50 ml) was heated and stirred at 80° C. for 24 hrs. Reaction mixture was then cooled and diluted with water (500 ml), acidified with 1N HCl and extracted with ethyl acetate (3×100 ml). The ethyl acetate extract was washed 5% sodium bicarbonate and brine and dried over anhydrous sodium sulfate. The dried extract on concentration afforded a residue which was purified by silica gel chromatography using 10% ethyl acetate in petroleum ether as the eluent to provide 5.0 gm of the title product as white solid. mp: 87-89° C.

후처리

  1. temperaturewas heated
  2. customReaction mixture
  3. temperaturewas then cooled
  4. extractionextracted with ethyl acetate (3×100 ml)
  5. extractionThe ethyl acetate extract
  6. washwas washed 5% sodium bicarbonate and brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. extractionThe dried extract on concentration
  9. customafforded a residue which
  10. customwas purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-090b96ab78684a2ba796cb9117c35e13
출처 데이터셋
uspto-grants-2008_06
특허 번호
US07384962B2

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