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Benzoate → Hexan-2-yl 4-hydroxybenzoate

HRID 2379656
ノート
印刷プレビュー

反応式

HRID 2379656 の反応式
[C:1]([O-:9])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:10](N)[C:11]1C=[CH:15][CH:14]=[CH:13][CH:12]=1.ClCCl.C([OH:23])C>>[OH:23][C:5]1[CH:6]=[CH:7][C:2]([C:1]([O:9][CH:14]([CH3:15])[CH2:13][CH2:12][CH2:11][CH3:10])=[O:8])=[CH:3][CH:4]=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 4

HCID 242BenzoateHCID 702EthanolHCID 6344DichloromethaneHCID 7504Benzylamine

生成物 1

HCID 19365253Hexan-2-yl 4-hydroxybenzoate収率 100%

実験手順

Said benzoate (4.7 mmols) was dissolved in 20 ml of ethanol, and 9.7 mmols of benzylamine were added. The mixture was stirred overnight. To the reaction mixture was added 50 ml of dichloromethane. The organic layer was washed with a hydrochloric acid aqueous solution and water in this sequence. Subsequently, the organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated. The obtained crude product was purified by silica gel column chromatography to afford 1-methylpentyl p-hydroxybenzoate in a yield of 100%.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. washThe organic layer was washed with a hydrochloric acid aqueous solution and water in this sequence
  2. dry with materialSubsequently, the organic layer was dried over anhydrous sodium sulfate
  3. customthe solvent was evaporated
  4. customThe obtained crude product
  5. customwas purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-ce11df50853249ce974cb5e7a04889ad
出典データセット
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05364560

反応ノート

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