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2-(Trimethylsilyl)ethanol → HCID 19756384, 화합물

HRID 893621
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HRID 893621 반응식
CC(C)([O-])C.[K+].[CH3:7][Si:8]([CH3:13])([CH3:12])[CH2:9][CH2:10][OH:11].Cl[C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][N:16]=1>CN(C=O)C>[N+:21]([C:18]1[CH:19]=[CH:20][C:15]([O:11][CH2:10][CH2:9][Si:8]([CH3:13])([CH3:12])[CH3:7])=[N:16][CH:17]=1)([O-:23])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 180132-(Trimethylsilyl)ethanolHCID 783082-Chloro-5-nitropyridineHCID 23665647Potassium tert-butoxide

생성물 1

HCID 19756384HCID 19756384, 화합물수율 82.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Potassium t-butoxide (25.8 g) was added portionwise over 20 minutes to a solution of 2-(trimethylsilyl)ethanol (20.8 g) and 2-chloro-5-nitropyridine (27.8 g) in DMF (170 ml). The mixture was stirred for 18 hours and then poured into ice-water (900 ml). The mixture was extracted with ethyl acetate (3×300 ml) and the extracts were washed with water (200 ml), followed by saturated sodium chloride solution (200 ml) and dried (MgSO4). Volatile material was removed by evaporation to give 5-nitro-2-[2-(trimethylsilyl)ethoxy]pyridine (34.9 g) as an oil; NMR: 0.05(s,9H), 1.1-1.2(m,2H), 4.45-4.55(m,2H), 6.75(d,1H), 8.3(dd,1H), 9.05(d,1H).

후처리

  1. extractionThe mixture was extracted with ethyl acetate (3×300 ml)
  2. washthe extracts were washed with water (200 ml)
  3. dry with materialdried (MgSO4)
  4. customVolatile material was removed by evaporation

출처 및 근거

ORD 기록
ord-83d5a301a0a64cd8ac9b1022e6029934
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05126344

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