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

HRID 2076042
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HRID 2076042 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

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

생성물 1

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

실험 절차

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)+].

후처리

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

출처 및 근거

ORD 기록
ord-9b799946d1694e1c83eaed6749e7fbbf
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07923450B2

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