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Sulfur Dioxide → Lithium 4-methyl-3-thiophenesulfinate

HRID 1248378
ノート
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反応式

HRID 1248378 の反応式
Br[C:2]1[C:6]([CH3:7])=[CH:5][S:4][CH:3]=1.C([Li:12])CCC.[S:13](=[O:15])=[O:14]>C(OCC)C.CCCCCC>[CH3:7][C:6]1[C:2]([S:13]([O-:15])=[O:14])=[CH:3][S:4][CH:5]=1.[Li+:12]
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 1119Sulfur DioxideHCID 27349353-Bromo-4-methylthiopheneHCID 178418339Butyllithium

生成物 1

HCID 23669555Lithium 4-methyl-3-thiophenesulfinate

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 8058Hexane溶媒

実験手順

To 30 g of 3-bromo-4-methylthiophene in 150 ml of anhydrous ethyl ether under nitrogen at -70° to -75° C. was added, cautiously, during 30 minutes 111 ml of 1.6M butyl lithium in hexane. The mixture was stirred for an additional thirty minutes and then 30 ml of liquified sulfur dioxide was added at such a rate that the temperature of the reaction mixture was maintained below -70° C. Upon completion of the addition, the mixture was stirred for an additional 90 minutes at -75° C. and then allowed to stand overnight at room temperature. The resulting precipitate was filtered and washed with ethyl ether, dried in air and in vacuo under nitrogen to yield 30 g of the desired salt, m.p. >250° C.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturewas maintained below -70° C
  2. additionUpon completion of the addition
  3. stirringthe mixture was stirred for an additional 90 minutes at -75° C.
  4. filtrationThe resulting precipitate was filtered
  5. washwashed with ethyl ether
  6. customdried in air and in vacuo under nitrogen

出典と根拠

ORDレコード
ord-9c83418814a64a63b686491b5acf7391
出典データセット
uspto-grants-1985_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04523943

反応ノート

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