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Potassium Hydroxide → 2-(2,4-dichlorophenoxy)-2-methylpropanoic acid

HRID 1400241
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HRID 1400241 반응식
[OH-].[K+].[Cl:3][C:4]1[CH:18]=[C:17]([Cl:19])[CH:16]=[CH:15][C:5]=1[O:6][C:7]([CH3:14])([CH3:13])[C:8]([O:10]CC)=[O:9]>O.CCO>[Cl:3][C:4]1[CH:18]=[C:17]([Cl:19])[CH:16]=[CH:15][C:5]=1[O:6][C:7]([CH3:14])([CH3:13])[C:8]([OH:10])=[O:9]
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참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 682839HCID 682839, 화합물2회

생성물 1

HCID 2514232-(2,4-dichlorophenoxy)-2-methylpropanoic acid

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

To a solution of KOH (2.48 g, 44.2 mmol, 15 eq) in H2O (12 mL) was added a solution of ethyl 2-(2,4-dichlorophenoxy)-2-methylpropionate (compound 5; 0.80 g, 2.89 mmol) in EtOH (12 mL). The solution was stirred at room temperature for 4 hours, then excess EtOH was removed under vacuum. The remaining aqueous solution was washed with EtOAc (10 mL), then acidified with concentrated aqueous HCl. The aqueous mixture was then extracted with EtOAc (10 mL), and the organic extract dried over Na2SO4, filtered, and evaporated to yield a thick, colorless oil which was used without further purification: 1H NMR (CDCl3) δ 7.42-7.41 (d, 1H), 7.19-7.15 (dd, 1H), 7.04-7.01 (d, 1H), 1.64 (s, 6H).

후처리

  1. customexcess EtOH was removed under vacuum
  2. washThe remaining aqueous solution was washed with EtOAc (10 mL)
  3. extractionThe aqueous mixture was then extracted with EtOAc (10 mL)
  4. extractionthe organic extract
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. customevaporated
  8. customto yield a thick, colorless oil which
  9. customwas used without further purification

출처 및 근거

ORD 기록
ord-b275cd786f6e4ed3b9c392a411fcac84
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08906945B2

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