Potassium Carbonate → 3-Cyclopentyl-propyl (2,2-dimethoxy-ethyl)-amine

HRID 1071165노트

반응식

HRID 1071165 반응식
[CH3:1][O:2][CH:3]([O:6][CH3:7])[CH2:4][NH2:5].C(=O)([O-])[O-].[K+].[K+].[CH:14]1([CH2:19][CH2:20][CH2:21]I)[CH2:18][CH2:17][CH2:16][CH2:15]1>CN(C)C=O>[CH:14]1([CH2:19][CH2:20][CH2:21][NH:5][CH2:4][CH:3]([O:6][CH3:7])[O:2][CH3:1])[CH2:18][CH2:17][CH2:16][CH2:15]1

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 89728Aminoacetaldehyde dimethyl acetalHCID 15508337(3-Iodopropyl)cyclopentane

생성물 1

HCID 187930233-Cyclopentyl-propyl (2,2-dimethoxy-ethyl)-amine수율 89.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 2-aminoacetaldehyde dimethyl acetal (3.0 mL, 27.5 mmol), solid potassium carbonate (2.1 g, 15.2 mmol), and 3-cyclopentyl-1-iodopropane (3.3 g, 13.9 mmol) in anhydrous N,N-dimethylformamide was stirred for 12 hours at room temperature. The mixture was filtered, and the filtrate was partitioned between water and ethyl acetate. The organic layer was washed with brine, dried (Na2SO4) and concentrated to a crude oil. The crude was passed through a plug of silica gel with ethyl acetate to provide a yellow oil (2.67 g, 89%). 1H NMR (300 MHz, DMSO-d6) δ 4.35 (t, 1H), 3.23 (s, 6H), 2.54 (d, 2H), 1.70 (m, 3H), 1.51 (m, 6H), 1.36 (m, 2H), 1.27 (m, 2H), 1.04 (m, 2H).

후처리

  1. filtrationThe mixture was filtered
  2. customthe filtrate was partitioned between water and ethyl acetate
  3. washThe organic layer was washed with brine
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated to a crude oil

출처 및 근거

ORD 기록
ord-bdc9be844bf34f4ebf1074f08834c5f6
출처 데이터셋
uspto-grants-2005_06
특허 번호
US06903218B2

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