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Sulfuric Acid → 4-(Dimethylamino)-4-(4-methoxyphenyl)cyclohexan-1-one

HRID 1477203
ノート
印刷プレビュー

反応式

HRID 1477203 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2([N:19]([CH3:21])[CH3:20])[CH2:18][CH2:17][C:12]3(OCC[O:13]3)[CH2:11][CH2:10]2)=[CH:5][CH:4]=1.OS(O)(=O)=O>CCOCC>[CH3:20][N:19]([CH3:21])[C:9]1([C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=2)[CH2:18][CH2:17][C:12](=[O:13])[CH2:11][CH2:10]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 1118Sulfuric AcidHCID 12595623[8-(4-Methoxy-phenyl)-1,4-dioxa-spiro[4.5]dec-8-yl]-dimethylamine

生成物 1

HCID 125956454-(Dimethylamino)-4-(4-methoxyphenyl)cyclohexan-1-one

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

The title compound from step 1 (6.80 g, 23 mmol) was dissolved in ether (100 mL), mixed with 5% H2SO4 (100 mL) and the solution vigorously stirred for 2 d at RT. The phases were separated and the ether phase discarded. The aqueous phase was made alkaline with 5N NaOH with ice cooling and extracted three times with ether, the combined organic phases were then washed with water, dried over Na2SO4 and concentrated to low volume in a vacuum.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThe phases were separated
  2. extractionextracted three times with ether
  3. washthe combined organic phases were then washed with water
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated to low volume in a vacuum

出典と根拠

ORDレコード
ord-c10b10251abf48cd8b2c3487177669e2
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09403767B2

反応ノート

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