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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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5-Methoxybicyclo[4.2.0]octa-1,3,5-trien-7-one → Bicyclo[4.2.0]octa-1,3,5-trien-7-ol, 5-methoxy-

HRID 1872095
ノート
印刷プレビュー

反応式

HRID 1872095 の反応式
[BH4-].[Na+].[CH3:3][O:4][C:5]1[C:10]2[C:11](=[O:13])[CH2:12][C:9]=2[CH:8]=[CH:7][CH:6]=1>CO>[CH3:3][O:4][C:5]1[C:10]2[CH:11]([OH:13])[CH2:12][C:9]=2[CH:8]=[CH:7][CH:6]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 27527445-Methoxybicyclo[4.2.0]octa-1,3,5-trien-7-oneHCID 4311764Sodium borohydride

生成物 1

HCID 10103323Bicyclo[4.2.0]octa-1,3,5-trien-7-ol, 5-methoxy-収率 67%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
0 °C

実験手順

13.21 g (0.35 mol) of sodium borohydride are added in small fractions to a solution, maintained at 0° C., of 42.8 g (0.29 mol) of 6-methoxybenzocyclobutan-1-one in 1.5 liters of methanol. The temperature is maintained at 0° C. for 2 hours. After returning to room temperature, the reaction mixture is evaporated to dryness and then taken up in water. The aqueous phase is extracted several times with ethyl acetate. The organic phases are combined, washed with brine, dried over MgSO4, filtered and evaporated to yield, after chromatography on silica, 29.2 g of the expected product in the form of a solid, the melting point of which is 71-73° C.

後処理

  1. customAfter returning to room temperature
  2. customthe reaction mixture is evaporated to dryness
  3. extractionThe aqueous phase is extracted several times with ethyl acetate
  4. washwashed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated
  8. customto yield

出典と根拠

ORDレコード
ord-eb337e61c1ce4e36971446a5f7b74f13
出典データセット
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06107345

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート