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

HRID 1758985
ノート
印刷プレビュー

反応式

HRID 1758985 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-79ef9a6af00d412fb24e917f96ff718c
出典データセット
uspto-grants-1982_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04338333

反応ノート

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