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tert-Butoxy bis(dimethylamino)methane → 6-[1-Dimethylamino-methylidene]-2-methyl-2-phenylcyclohexanone

HRID 2076042
ノート
印刷プレビュー

反応式

HRID 2076042 の反応式
[CH3:1][C:2]1([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:7][CH2:6][CH2:5][CH2:4][C:3]1=[O:8].C(O[CH:20](N(C)C)[N:21]([CH3:23])[CH3:22])(C)(C)C>>[CH3:20][N:21]([CH3:23])[CH:22]=[C:4]1[C:3](=[O:8])[C:2]([CH3:1])([C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:7][CH2:6][CH2:5]1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 79885tert-Butoxy bis(dimethylamino)methaneHCID 3499432-Methyl-2-phenylcyclohexanone

生成物 1

HCID 670961136-[1-Dimethylamino-methylidene]-2-methyl-2-phenylcyclohexanone収率 101.9%

実験手順

A mixture 2-methyl-2-phenylcyclohexanone (94 mg, 0.5 mmol) and tert.-butoxy-bis-(dimethylamino)-methane (0.16 mL, 0.77 mmol) was stirred at 110° C. for 1.5 h, whereupon it was cooled and evaporated under reduced pressure. Toluene (3 mL) was added to the residue and the solution was evaporated again to give the title compound (124 mg) as red oil which was used without further purification. MS ISP (m/e): 244.4 [(M+H)+].

後処理

  1. temperaturewas cooled
  2. customevaporated under reduced pressure
  3. additionToluene (3 mL) was added to the residue
  4. custom
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
the solution was evaporated again

出典と根拠

ORDレコード
ord-9b799946d1694e1c83eaed6749e7fbbf
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07923450B2

反応ノート

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