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Water → HCID 19849494、化合物

HRID 1607817
ノート
印刷プレビュー

反応式

HRID 1607817 の反応式
[OH-].[Na+].[C:3]1([OH:9])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[O:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]1[O:16][CH2:17][C:18]#[C:19][CH2:20]Br.O>C(O)C>[O:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]1[O:16][CH2:17][C:18]#[C:19][CH2:20][O:9][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=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 4

HCID 962WaterHCID 996PhenolHCID 14798Sodium HydroxideHCID 113682802-(4-Bromobut-2-ynoxy)tetrahydropyran

生成物 1

HCID 19849494HCID 19849494、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

1.10 g of sodium hydroxide was added to a solution of 2.35 g of phenol in 20 ml of absolute ethanol. The mixture was refluxed until complete dissolution, then 2.92 g of 1-bromobut-2-yn-4-ol tetrahydropyranyl ether was added. The reflux was resumed for 2 additional hours. It was then cooled, poured into water and extracted with ether (3×50 ml). The organic extracts were washed with 20% aqueous sodium hydroxide solution and water, dried over sodium sulfate and evaporated in vacuo. The residue was purified by column chromatography on 50 g of silica gel, using hexane:ethyl acetate (98:2) as eluant, to yield 4-phenoxy-but-2-yn-1-ol tetrahydropyranyl ether, as an oil.

後処理

  1. temperatureThe mixture was refluxed until complete dissolution
  2. temperatureIt was then cooled
  3. extractionextracted with ether (3×50 ml)
  4. washThe organic extracts were washed with 20% aqueous sodium hydroxide solution and water
  5. dry with materialdried over sodium sulfate
  6. customevaporated in vacuo
  7. customThe residue was purified by column chromatography on 50 g of silica gel

出典と根拠

ORDレコード
ord-0b3ed928a3ee4f049fffa71576773fc0
出典データセット
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04867915

反応ノート

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