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3-(4-Methyl-tetrahydro-pyran-4-yl)-acrylic acid ethyl ester → HCID 67528472、化合物

HRID 1512177
ノート
印刷プレビュー

反応式

HRID 1512177 の反応式
C([O:3][C:4](=[O:14])[CH:5]=[CH:6][C:7]1([CH3:13])[CH2:12][CH2:11][O:10][CH2:9][CH2:8]1)C>CCO.[OH-].[Na+]>[CH3:13][C:7]1([CH:6]=[CH:5][C:4]([OH:14])=[O:3])[CH2:12][CH2:11][O:10][CH2:9][CH2:8]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 675281893-(4-Methyl-tetrahydro-pyran-4-yl)-acrylic acid ethyl ester

生成物 1

HCID 67528472HCID 67528472、化合物

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 14798Sodium Hydroxide溶媒

実験手順

To a solution of 3-(4-methyl-tetrahydro-pyran-4-yl)-acrylic acid ethyl ester (396 mg, 2.00 mmol, prepared as in STEP A above) in EtOH (10 mL), 6N aqueous NaOH (1 mL) was added dropwise. The resulting mixture was stirred at room temperature over night. The resulting mixture was concentrated and the resulting residue was dissolved in 20 mL of water. The resulting solution was washed twice with diethyl ether (10 mL), and the aqueous layer was acidified with 6N HCl and extracted thrice with DCM (20 mL). The DCM layers were combined, dried over Na2SO4 and concentrated in vacuo to yield 3-(4-methyl-tetrahydro-pyran-4-yl)-acrylic acid, which was used in next step without further purification.

後処理

  1. concentrationThe resulting mixture was concentrated
  2. dissolutionthe resulting residue was dissolved in 20 mL of water
  3. washThe resulting solution was washed twice with diethyl ether (10 mL)
  4. extractionextracted thrice with DCM (20 mL)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-5c99a39bf5874d8890088b5beea8bb30
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08217060B2

反応ノート

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