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2-Iodobutane → HCID 69551882, 화합물

HRID 1833242
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HRID 1833242 반응식
[CH3:1][O:2][C:3](=[O:12])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([OH:11])[CH:6]=1.I[CH:14]([CH2:16][CH3:17])[CH3:15].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH3:1][O:2][C:3](=[O:12])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH:14]([CH2:16][CH3:17])[CH3:15])[CH:6]=1
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참가 물질

5

반응물 3

HCID 105592-IodobutaneHCID 11430Potassium CarbonateHCID 39129Methyl 3-Hydroxyphenylacetate

생성물 1

HCID 69551882HCID 69551882, 화합물

시약·촉매·용매 1

HCID 180Acetone용매

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온도
65 °C

실험 절차

To 3-hydroxyphenyl acetic acid methyl ester (27.3 g, 165 mmol) in acetone (200 mL) was added 2-iodobutane (55 mL, 478 mmol) and potassium carbonate (83 g, 601 mmol). The mixture was heated at 65° C. for 48 hrs and filtered through a Celite® pad. The filtrate was concentrated in vacuo and the residue was diluted with dichloromethane and water. The aqueous phase was extracted with dichloromethane (3×100 mL). The combined extracts were washed with saturated sodium chloride (50 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford (3-sec-butoxy-phenyl)-acetic acid methyl ester. To a solution of (3-sec-butoxy-phenyl)-acetic acid methyl ester in methanol (200 mL) was added 10N sodium hydroxide solution (50 mL). The reaction mixture was stirred at 60° C. for 4 hrs. The solvent was evaporated and the mixture was acidified to pH=3 by addition of 6N hydrogen chloride solution. The aqueous phase was extracted with dichloromethane (3×100 m]L). The combined extracts were washed with saturated aqueous sodium chloride solution (80 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford (3-sec-butoxy-phenyl) acetic acid (25 g, 73% yield) as a light brown oil.

후처리

  1. filtrationfiltered through a Celite® pad
  2. concentrationThe filtrate was concentrated in vacuo
  3. additionthe residue was diluted with dichloromethane and water
  4. extractionThe aqueous phase was extracted with dichloromethane (3×100 mL)
  5. washThe combined extracts were washed with saturated sodium chloride (50 mL)
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-5ce1b38e06974575a270ff29d1ea8f78
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067529B2

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