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Potassium Hydroxide → 4-phenyltetrahydro-2H-pyran-4-carboxylic acid

HRID 2078292
ノート
印刷プレビュー

反応式

HRID 2078292 の反応式
[C:1]1([C:7]2([C:13]([O:15]C)=[O:14])[CH2:12][CH2:11][O:10][CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[K+]>CCO.C(OCC)C>[C:1]1([C:7]2([C:13]([OH:15])=[O:14])[CH2:8][CH2:9][O:10][CH2:11][CH2:12]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14797Potassium HydroxideHCID 20110318HCID 20110318、化合物

生成物 1

HCID 41385534-phenyltetrahydro-2H-pyran-4-carboxylic acid収率 80.3%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 3283Diethyl Ether溶媒

実験手順

Methyl 4-phenyl-tetrahydro-2H-pyran-4-carboxylate (15.4 g, 69.9 mmol) was dissolved in EtOH (100 mL). KOH (39.2 g, 699 mmol) was then added. The reaction mixture was then heated at reflux for 2 hours and then cooled to ambient temperature, diluted with 150 mL of diethyl ether, added to a separatory funnel, partitioned with water, washed 2 times with 50 mL of water, and separated. The aqueous layer was acidified to a pH of 2 with concentrated HCl and extracted with CHCl3 (3×100 mL), dried over Na2SO4, and concentrated in vacuo to give the title compound (11.58 g) as a light yellow solid. MS m/e=229 (M+Na)+.

後処理

  1. temperatureThe reaction mixture was then heated
  2. temperatureat reflux for 2 hours
  3. additionadded to a separatory funnel
  4. custompartitioned with water
  5. washwashed 2 times with 50 mL of water
  6. customseparated
  7. extractionextracted with CHCl3 (3×100 mL)
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-7b82e36608a0466b99f3a4b2861f7d6b
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07928139B2

反応ノート

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