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Sodium Hydroxide → 4-Cyclopropyl-2-methylbenzoic acid

HRID 2069827
ノート
印刷プレビュー

反応式

HRID 2069827 の反応式
[CH:1]1([C:4]2[CH:13]=[CH:12][C:7]([C:8]([O:10]C)=[O:9])=[C:6]([CH3:14])[CH:5]=2)[CH2:3][CH2:2]1.[OH-].[Na+]>CO>[CH:1]1([C:4]2[CH:13]=[CH:12][C:7]([C:8]([OH:10])=[O:9])=[C:6]([CH3:14])[CH:5]=2)[CH2:2][CH2:3]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 2

HCID 14798Sodium HydroxideHCID 59020660Methyl 4-cyclopropyl-2-methylbenzoate

生成物 1

HCID 590206584-Cyclopropyl-2-methylbenzoic acid収率 100%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Methyl 4-cyclopropyl-2-methylbenzoate (32.00 g, 168 mmol), 250 mL of 5 M aqueous sodium hydroxide, and 150 mL of methanol were stirred at 85° for 18 hr. Cooled the reaction mixture to room temperature and concentrated in vacuo. Dissolved the white residue in 500 mL of water, cooled the solution in an ice bath, and added 120 mL of concentrated hydrochloric acid. A white precipitate formed. Extracted the aqueous mixture with 2×250 mL EtOAc. Combined the organic extracts and washed with 250 mL brine. Dried the solution over MgSO4 and concentrated in vacuo to obtain 4-cyclopropyl-2-methylbenzoic acid as an off-white solid (29.52 g, 168 mmol). MS (ESI) MS (ESI) 175.0 (M-H)−.

後処理

  1. concentrationconcentrated in vacuo
  2. dissolutionDissolved the white residue in 500 mL of water
  3. temperaturecooled the solution in an ice bath
  4. additionadded 120 mL of concentrated hydrochloric acid
  5. customA white precipitate formed
  6. extractionExtracted the aqueous mixture with 2×250 mL EtOAc
  7. washwashed with 250 mL brine
  8. dry with materialDried the solution over MgSO4
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-707cce3dfa444b37bb672d7d3aed6038
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08299077B2

反応ノート

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