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Methanol → 2-Furanol, tetrahydro-5-phenyl-

HRID 716160
ノート
印刷プレビュー

反応式

HRID 716160 の反応式
[H-].C([Al+]CC(C)C)C(C)C.C1(C)C=CC=CC=1.[C:18]1([CH:24]2[O:28][C:27](=[O:29])[CH2:26][CH2:25]2)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.CO.C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>C1(C)C=CC=CC=1>[C:18]1([CH:24]2[O:28][CH:27]([OH:29])[CH2:26][CH2:25]2)[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=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 887MethanolHCID 13884gamma-Phenyl-gamma-butyrolactoneHCID 9855836Potassium sodium tartarateHCID 86583787Diisobutylaluminumhydride toluene

生成物 1

HCID 111163882-Furanol, tetrahydro-5-phenyl-収率 96.8%

試薬・触媒・溶媒 1

HCID 1140Toluene
溶媒

実験手順

4.1 mL of a 1.5 mol/L diisobutylaluminum hydride/toluene solution was added dropwise to a solution of 1.0 g of 5-phenyloxolane-2-one in 12 mL of toluene at −60° C., and the obtained mixture was then stirred for 30 minutes. Thereafter, 1 mL of methanol was added to the reaction mixture, and thereafter, 40 mL of a 20% potassium sodium tartrate aqueous solution was then added to the mixture at room temperature. The thus obtained mixture was stirred for 1 hour. Thereafter, the water layer was removed, and the solvent was then distilled away under reduced pressure, so as to obtain 0.98 g of 5-phenyloxolan-2-ol in the form of a colorless oily product.

後処理

  1. stirringThe thus obtained mixture was stirred for 1 hour
  2. customThereafter, the water layer was removed
  3. distillationthe solvent was then distilled away under reduced pressure

出典と根拠

ORDレコード
ord-96a947dfe0754fc7aafad94113073dd8
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09187514B2

反応ノート

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