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Carbonic Acid → 2-Hydroxy-2,4-dimethyl-3-pentanone

HRID 648343
ノート
印刷プレビュー

反応式

HRID 648343 の反応式
[CH3:1][CH:2]([C:4](=[O:8])[CH:5]([CH3:7])[CH3:6])[CH3:3].BrBr.[OH:11]C(O)=O>C(Cl)(Cl)Cl>[OH:11][C:2]([CH3:3])([C:4](=[O:8])[CH:5]([CH3:7])[CH3:6])[CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 767Carbonic AcidHCID 112712,4-Dimethyl-3-pentanoneHCID 24408Bromine

生成物 1

HCID 5477352-Hydroxy-2,4-dimethyl-3-pentanone

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

To a stirred solution of 28.3 ml. (0.2 mole) 2,4-dimethyl-3-pentanone in 100 ml. chloroform was added dropwise 10.3 ml. (0.2 mole) bromine in 30 ml. of the same solvent. The resulting mixture was stirred for a few minutes, the solvent evaporated in vacuo, the residue taken up in 100 ml. ethanol. Water, 50 ml., and 10 M sodium hydroxide, 50 ml., added. The resulting mixture was stirred at reflux for one hour, diluted with 200 ml. water and extracted with 3×50 ml. ethyl ether. The extracts were dried (MgSO4) evaporated to dryness and the residue distilled to obtain 15.95 g. (61%) of the hydroxy-ketone, b.p. 60°-62° C./18 mm.

後処理

  1. customthe solvent evaporated in vacuo
  2. addition, added
  3. stirringThe resulting mixture was stirred
  4. temperatureat reflux for one hour
  5. additiondiluted with 200 ml
  6. extractionwater and extracted with 3×50 ml
  7. dry with materialThe extracts were dried (MgSO4)
  8. customevaporated to dryness
  9. distillationthe residue distilled
  10. customto obtain 15.95 g

出典と根拠

ORDレコード
ord-d03a9a3d122b4d058353165d01cba6ef
出典データセット
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04411925

反応ノート

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