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Potassium Hydroxide → 2-(Benzyloxy)-5-hydroxybenzoic acid

HRID 1623660
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HRID 1623660 반응식
CC1C=CC(S([O:11][C:12]2[CH:13]=[CH:14][C:15]([O:22][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)=[C:16]([CH:21]=2)[C:17]([O:19]C)=[O:18])(=O)=O)=CC=1.[OH-].[K+]>C(O)C.O>[OH:11][C:12]1[CH:13]=[CH:14][C:15]([O:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)=[C:16]([CH:21]=1)[C:17]([OH:19])=[O:18]
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참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 86762539Methyl 5-{[(4-methylphenyl)sulfonyl]oxy}-2-[(phenylmethyl)oxy]benzoate

생성물 1

HCID 247719442-(Benzyloxy)-5-hydroxybenzoic acid

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

Methyl 5-{[(4-methylphenyl)sulfonyl]oxy}-2-[(phenylmethyl)oxy]benzoate (may be prepared as described in Description 37; 2.5 g, 6.06 mmol) was boiled with potassium hydroxide (2.38 g, 42.4 mmol) in a mixture of ethanol (60 ml) and water (15 ml) for 4 h. After the ethanol had been evaporated, the aqueous solution was washed with ethyl acetate (20 ml) and acidified with concentrated HCl. The mixture was extracted with ethyl acetate (3×30 ml). The organic phase was washed with saturated brine (25 ml), dried over sodium sulphate and evaporated in vacuo to yield the title compound as a yellow oil. 1.35 g.

후처리

  1. customAfter the ethanol had been evaporated
  2. washthe aqueous solution was washed with ethyl acetate (20 ml)
  3. extractionThe mixture was extracted with ethyl acetate (3×30 ml)
  4. washThe organic phase was washed with saturated brine (25 ml)
  5. dry with materialdried over sodium sulphate
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-396329d062ac425c8aa7258764818e9a
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08778939B2

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