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Hydroquinone → 4-(6'-Methyloctyloxy)phenol

HRID 986098
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반응식

HRID 986098 반응식
[C:1]1([CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1)[OH:2].Br[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH:15]([CH3:18])[CH2:16][CH3:17].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH3:18][CH:15]([CH2:16][CH3:17])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][O:2][C:1]1[CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 785HydroquinoneHCID 11430Potassium CarbonateHCID 135481051-Bromo-6-methyloctane

생성물 1

HCID 230392144-(6'-Methyloctyloxy)phenol

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A 25 ml-flask was charged with 0.637 g of hydroquinone, 1 g of optically active 1-bromo-6-methyloctane, 0.667 g of anhydrous potassium carbonate and 4 ml of N,N-dimethylformamide, and reaction was carried out at 90° C. for 9.5 hours. After the reaction, insoluble substances were recovered by filtration and extracted with ether. The ether layer was washed with water and a saturated aqueous solution of sodium chloride and dried, and ether was removed by distillation under reduced pressure. The obtained crude product was purified by silica gel chromatography to obtain 0.32 g of optically active 4-(6'-methyloctyloxy)phenol.

후처리

  1. customAfter the reaction, insoluble substances
  2. filtrationwere recovered by filtration
  3. extractionextracted with ether
  4. washThe ether layer was washed with water
  5. dry with materiala saturated aqueous solution of sodium chloride and dried
  6. customether was removed by distillation under reduced pressure
  7. customThe obtained crude product
  8. customwas purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-c9ba37f1d3f84863bd1d24e907df54ec
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04710585

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