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Chlorotrimethylsilane → 5,6,7,8-Tetrahydro-8-trimethylsilyl-3-methylquinoline

HRID 482972
ノート
印刷プレビュー

反応式

HRID 482972 の反応式
[CH3:1][C:2]1[CH:3]=[N:4][C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:10]=2[CH:11]=1.C([Li])CCC.[CH3:17][Si:18](Cl)([CH3:20])[CH3:19]>CCCCCC.O1CCCC1>[CH3:17][Si:18]([CH3:20])([CH3:19])[CH:6]1[C:5]2[N:4]=[CH:3][C:2]([CH3:1])=[CH:11][C:10]=2[CH2:9][CH2:8][CH2:7]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6397ChlorotrimethylsilaneHCID 1200283-Methyl-5,6,7,8-tetrahydroquinolineHCID 178418339Butyllithium

生成物 1

HCID 202445185,6,7,8-Tetrahydro-8-trimethylsilyl-3-methylquinoline収率 91%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒3 回HCID 8058
Hexane
溶媒

実験手順

A mixture of 5,6,7,8-tetrahydro-3-methylquinoline (29.4 g, 0.2 M) and tetrahydrofuran (THF) (50 ml) was added to a mixture of a 1.55 molar solution of butyl lithium in hexane (129 ml, 0.2 M) and THF (50 ml), maintained below 10°. After 0.5 hour the mixture was blown over by inert gas onto a mixture of trimethylsilyl chloride (50 ml, 0.4 M) in the THF (100 ml), maintained below 10°. After 0.5 hour, the mixture was evaporated and the residue extracted with hexane. The hexane extracts were evaporated with the residue distilled to give the title compound (40 g, 91%) b.p. 118°-124°/5 mbar. (Found: C70.9; H,9.65; N,6.4% C13H21NSi requires: C,71.2; H,9.6; N6.4%).

後処理

  1. temperaturemaintained below 10°
  2. temperaturemaintained below 10°
  3. customthe mixture was evaporated
  4. extractionthe residue extracted with hexane
  5. customThe hexane extracts were evaporated with the residue
  6. distillationdistilled

出典と根拠

ORDレコード
ord-78a9d0b885624a679eb568879c81147d
出典データセット
uspto-grants-1986_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04577022

反応ノート

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