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Ammonium fluoride → Methyl 5-hydroxy-2-methoxybenzoate

HRID 637219
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HRID 637219 반응식
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]([O:13][Si](C(C)(C)C)(C)C)=[CH:9][C:4]=1[C:5]([O:7][CH3:8])=[O:6].[F-].[NH4+]>CO>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][C:4]=1[C:5]([O:7][CH3:8])=[O:6]
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참가 물질

4

반응물 2

HCID 25516Ammonium fluorideHCID 18464864Methyl 2-methoxy-5-(t-butyldimethylsilyloxy)benzoate

생성물 1

HCID 592162Methyl 5-hydroxy-2-methoxybenzoate

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Combine methyl 2-methoxy-5-(t-butyldimethylsilyloxy)benzoate (11.1 g. 37.4 mmol) and ammonium fluoride (6.94 g, 0.187 mmol) in methanol (150 mL). Heat to reflux. After 1 hour, evaporate in vacuo to give a residue. Partition the residue between ethyl acetate and water, separate the layers, extract the organic layer with water and then brine. Dry the organic layer over MgSO4, filter, and evaporate in uacuo to give methyl 2-methoxy-5-hydroxybenzoate: mp; 110-112° C. Rf=0.27 (silica gel, 5% ethyl acetate/hexane).

후처리

  1. temperatureHeat to reflux
  2. customevaporate in vacuo
  3. customto give a residue
  4. customPartition the residue between ethyl acetate and water
  5. customseparate the layers
  6. extractionextract the organic layer with water
  7. dry with materialDry the organic layer over MgSO4
  8. filtrationfilter
  9. customevaporate in uacuo

출처 및 근거

ORD 기록
ord-cc63f7f2d2c947808406a91e56a6584e
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06194406B1

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