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Methanol → 4-Benzyloxymethyl-cyclohexanecarboxylic acid methyl ester

HRID 217238
ノート
印刷プレビュー

反応式

HRID 217238 の反応式
[CH2:1]([O:8][CH2:9][CH:10]1[CH2:15][CH2:14][CH:13]([CH:16]=[O:17])[CH2:12][CH2:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[O-]Cl.[Na+].[CH3:21][OH:22]>C(O)(=O)C>[CH3:21][O:22][C:16]([CH:13]1[CH2:12][CH2:11][CH:10]([CH2:9][O:8][CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:15][CH2:14]1)=[O:17]
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 3

HCID 887MethanolHCID 186672404-Benzyloxymethyl-cyclohexanecarbaldehydeHCID 23665760Sodium Hypochlorite

生成物 1

HCID 576866884-Benzyloxymethyl-cyclohexanecarboxylic acid methyl ester収率 65%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

4-Benzyloxymethyl-cyclohexanecarbaldehyde (1.70 g, 2.0 mmol) is dissolved in acetic acid (0.24 mL) and 2 mL of methanol. The reaction mixture is cooled to 0° C. to 5° C. and stirred while 10% NaOCl solution (2.5 mL, 4 mmol) is added dropwise over 20 minutes. The cooling bath is removed, and the mixture is allowed to come to room temperature. After addition of saturated aqueous NaHCO3, the mixture is extracted with EtOAc. The combined organic layer after dried over MgSO4 is concentrated to obtain 4-benzyloxymethyl-cyclohexanecarboxylic acid methyl ester as clear oil (343 mg, 65%) after purification.

後処理

  1. temperatureThe reaction mixture is cooled to 0° C. to 5° C.
  2. additionis added dropwise over 20 minutes
  3. customThe cooling bath is removed
  4. customto come to room temperature
  5. additionAfter addition of saturated aqueous NaHCO3
  6. extractionthe mixture is extracted with EtOAc
  7. dry with materialThe combined organic layer after dried over MgSO4
  8. concentrationis concentrated

出典と根拠

ORDレコード
ord-e8ac3f652ac6480f841de08b2cad4ba0
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08193349B2

反応ノート

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