Ammonia → 2-[4-(Aminomethyl)-3-methylphenyl]-2-methylpropanenitrile

HRID 603142노트

반응식

HRID 603142 반응식
[CH:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]([CH3:13])([CH3:12])[C:10]#[N:11])=[CH:5][C:4]=1[CH3:14])=O.[BH4-].[Na+].[NH3:17]>CO.CC(O[Ti](OC(C)C)(OC(C)C)OC(C)C)C>[NH2:17][CH2:1][C:3]1[CH:8]=[CH:7][C:6]([C:9]([CH3:13])([CH3:12])[C:10]#[N:11])=[CH:5][C:4]=1[CH3:14]

참가 물질

6

반응물 3

HCID 222AmmoniaHCID 4311764Sodium borohydrideHCID 582984532-(4-Formyl-3-methylphenyl)-2-methylpropanenitrile

생성물 1

HCID 582984482-[4-(Aminomethyl)-3-methylphenyl]-2-methylpropanenitrile수율 87%

시약·촉매·용매 2

HCID 178460666HCID 178460666, 화합물촉매HCID 887Methanol용매

실험 절차

2-(4-formyl-3-methylphenyl)-2-methylpropanenitrile 1.89 g, 10.2 mmol) is dissolved in 50 ml of 7M NH3 in MeOH. Ti(OiPr)4 (6 mmol, 20 mmol) is added and the mixture stirred for 3 hours at room temperature. NaBH4 (0.6 g, 15 mmol) is added and the reaction left at room temperature overnight. The mixture is quenched by the addition of 25 ml of NH4OH 2 M. The resulting precipitate is filtered off and washed with EtOAc. Phases are separated, the organic phase is dried over magnesium sulfate, filtered and evaporated to dryness, giving 2-[4-(aminomethyl)-3-methylphenyl]-2-methylpropanenitrile (1.325 g, 7.09 mmol, 87%). The crude product is used without further purification. 1H NMR (400 MHz, DMSO-D6) δ 1.64 (s, 6H, first rotamer) 1.65 (s, 6H, second rotamer) 2.28 (s, 3H, first rotamer) 2.29 (s, 3H, second rotamer) 3.32 (broad s, 2H) 3.67 (s, 2H, first rotamer) 3.68 (s, 2H, second rotamer) 7.24-7.27 (m, 1H) 7.28 (s, 1H) 7.36-7.40 (m, 1H).

후처리

  1. waitthe reaction left at room temperature overnight
  2. customThe mixture is quenched by the addition of 25 ml of NH4OH 2 M
  3. filtrationThe resulting precipitate is filtered off
  4. washwashed with EtOAc
  5. customPhases are separated
  6. dry with materialthe organic phase is dried over magnesium sulfate
  7. filtrationfiltered
  8. customevaporated to dryness

출처 및 근거

ORD 기록
ord-d137a0f6c75b4178ba2e7bbd98549db7
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07906654B2

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