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Hydrochloric Acid → 3'-Acetylaminomethylacetophenone

HRID 1734016
ノート
印刷プレビュー

反応式

HRID 1734016 の反応式
C([C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][CH:13]=1)[CH2:6][NH:7][C:8](=[O:10])[CH3:9])#N.C[Mg]Br.O.Cl.CC[O:21][CH2:22][CH3:23]>C(Cl)Cl.O1CCCC1>[C:8]([NH:7][CH2:6][C:5]1[CH:4]=[C:3]([C:22](=[O:21])[CH3:23])[CH:13]=[CH:12][CH:11]=1)(=[O:10])[CH3:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 962WaterHCID 3283Diethyl EtherHCID 19439673HCID 19439673、化合物HCID 178418573HCID 178418573、化合物

生成物 1

HCID 107977903'-Acetylaminomethylacetophenone

試薬・触媒・溶媒 2

HCID 6344
Dichloromethane
溶媒
HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of N-(3-cyanobenzyl)acetamide (7.7 g) in methylene dichloride (150 ml) and tetrahydrofuran (50 ml) was added dropwise a solution of methyl magnesium bromide in ether (3 mol/l, 52 ml) at 10° to 20° C. under stirring and the resulting mixture was stirred at the same condition for 6 hours. The reaction mixture was poured into water and the resultant mixture was adjusted to pH 7 with 6N hydrochloric acid and extracted with ethyl acetate. The extract was washed with brine and magnesium sulfate. The solvent was evaporated in vacuo and the residue was subjected to column chromatography on silica gel. The fractions eluted with a mixture of chloroform and ethyl acetate (8:2) were collected and the solvent was evaporated in vacuo to give 3'-(acetylaminomethyl)acetophenone (4.7 g) (oil).

後処理

  1. stirringthe resulting mixture was stirred at the same condition for 6 hours
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with brine and magnesium sulfate
  4. customThe solvent was evaporated in vacuo
  5. washThe fractions eluted with a mixture of chloroform and ethyl acetate (8:2)
  6. customwere collected
  7. customthe solvent was evaporated in vacuo

出典と根拠

ORDレコード
ord-6e0d0d76fc7e4cbb8631122fa976af01
出典データセット
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05532258

反応ノート

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