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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Methanesulfonic Acid → HCID 15422638、化合物

HRID 616624
ノート
印刷プレビュー

反応式

HRID 616624 の反応式
CS(O)(=O)=O.O[C:7]1[CH:12]=[CH:11][C:10]([C:13]2[C:17]3[CH:18]=[CH:19][C:20]([O:22][CH3:23])=[CH:21][C:16]=3[S:15][CH:14]=2)=[CH:9][CH:8]=1>>[C:10]1([C:13]2[C:17]3[CH:18]=[CH:19][C:20]([O:22][CH3:23])=[CH:21][C:16]=3[S:15][CH:14]=2)[CH:9]=[CH:8][CH:7]=[CH:12][CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 6395Methanesulfonic AcidHCID 22348372HCID 22348372、化合物

生成物 1

HCID 15422638HCID 15422638、化合物

実験手順

To 80 ml. of methanesulfonic acid (cooled to about 15° C.) were added 20.0 g. of the above product. The resulting mixture was stirred for two hours, and the dark red solution was poured over about 2 liters of ice. The mixture was extracted with 1 liter of ether. The ether extract was washed twice with 100 ml. of aqueous sodium chloride solution and once with 100 ml. of aqueous sodium bicarbonate solution. The ether layer was dried over magnesium sulfate, filtered, and evaporated to give an oil. The oil was crystallized from a mixture of ether and hexane to obtain 12.0 g. of 3-(4-hydroxyphenyl)-6-methoxybenzothiophene as white crystals, m.p. 140°-140.5° C.

後処理

  1. extractionThe mixture was extracted with 1 liter of ether
  2. extractionThe ether extract
  3. washwas washed twice with 100 ml
  4. dry with materialThe ether layer was dried over magnesium sulfate
  • filtrationfiltered
  • customevaporated
  • customto give an oil
  • customThe oil was crystallized from a mixture of ether and hexane
  • customto obtain 12.0 g
  • 出典と根拠

    ORDレコード
    ord-435d7d58e657488bac998d20b28106b2
    出典データセット
    uspto-grants-1978_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04075227

    反応ノート

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