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Diethyl Ether → HCID 12788084, 화합물

HRID 1732897
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반응식

HRID 1732897 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][N:8]([CH2:10][C:11]1[S:15][C:14]([CH2:16][O:17][CH2:18][C:19]([NH2:21])=O)=[CH:13][CH:12]=1)[CH3:9].CCOCC>O1CCCC1>[CH3:9][N:8]([CH2:10][C:11]1[S:15][C:14]([CH2:16][O:17][CH2:18][CH2:19][NH2:21])=[CH:13][CH:12]=1)[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 12788083HCID 12788083, 화합물HCID 21226445Aluminium lithium hydride

생성물 1

HCID 12788084HCID 12788084, 화합물수율 74.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A suspension of lithium aluminium hydride (0.38 g) and [[5-(N,N-dimethylaminomethyl)2-thienyl]methoxy]acetamide (2.28 g) in a mixture of dry ether (25 ml) and dry tetrahydrofuran (5 ml) was heated at reflux for 4 hr. The reaction was then quenched with water and evaporated. The residue was extracted with chloroform. The organic phase was dried and distilled to afford a colourless oil (1.6 g) b.p. 110°-120° (0.1 mm). NMR (CDCl3), 8.43, s, (2H); 7.72, s, (6H); 7.12, t, (2H); 6.46 t, (2H); 6.38, s, (2H); 5.32, s, (2H), 3-3.3, m, (2H).

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후처리

  1. temperaturewas heated
  2. temperatureat reflux for 4 hr
  3. customThe reaction was then quenched with water
  4. customevaporated
  5. extractionThe residue was extracted with chloroform
  6. customThe organic phase was dried
  7. distillationdistilled

출처 및 근거

ORD 기록
ord-72521e5fb5e94a56a837caf3710d7f1f
출처 데이터셋
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04239769

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