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Hydrochloric Acid → Methyl 2-(4-(2-oxopropyl)phenoxy)acetate

HRID 1758985
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HRID 1758985 반응식
S(S([O-])=O)([O-])(=O)=[O:2].[Na+].[Na+].[C:10]([CH2:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][C:23](=NO)[CH3:24])=[CH:18][CH:17]=1)([O:12][CH3:13])=[O:11].Cl>O.CO>[C:10]([CH2:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][C:23](=[O:2])[CH3:24])=[CH:18][CH:17]=1)([O:12][CH3:13])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 656671Sodium PyrosulfiteHCID 867384661-(4-Carbomethoxymethoxyphenyl)propan-2-one oxime

생성물 1

HCID 13851156Methyl 2-(4-(2-oxopropyl)phenoxy)acetate

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

Sodium metabisulphite (26 g) in water (60 ml) was added to 1-(4-carbomethoxymethoxyphenyl)propan-2-one oxime (7.5 g) in methanol (50 ml) and the mixture refluxed for 6 hours. The reaction mixture was cooled, concentrated hydrochloric acid (30 ml) added and the mixture extracted with ethyl acetate. The combined ethyl acetate extracts were washed with water followed by sodium bicarbonate solution. The ethyl acetate layer was dried (MgSO4) and evaporated to give the title compound as an oil which crystallised on standing, (mp 63°-70°l ). τ (CDCl3) 7.91 (3H, s), 6.30 (2H, s), 6.26 (3H, s), 5.42 (2H, s), 3.17 (2H, d, J=8 Hz), 2.87 (2H, d, J=8 Hz).

후처리

  1. temperaturethe mixture refluxed for 6 hours
  2. temperatureThe reaction mixture was cooled
  3. extractionthe mixture extracted with ethyl acetate
  4. washThe combined ethyl acetate extracts were washed with water
  5. dry with materialThe ethyl acetate layer was dried (MgSO4)
  6. customevaporated

출처 및 근거

ORD 기록
ord-79ef9a6af00d412fb24e917f96ff718c
출처 데이터셋
uspto-grants-1982_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04338333

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