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Phenylacetic Acid → Tert-butyl 2-phenylacetate

HRID 2276875
ノート
印刷プレビュー

反応式

HRID 2276875 の反応式
[C:1]1([CH2:7][C:8]([OH:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl(O)(=O)(=O)=O>C(OC(C)=O)(C)(C)C>[C:1]1([CH2:7][C:8]([O:10][C:1]([CH3:7])([CH3:6])[CH3:2])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=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 999Phenylacetic AcidHCID 24247Perchloric Acid

生成物 1

HCID 316203Tert-butyl 2-phenylacetate収率 137.1%

試薬・触媒・溶媒 1

HCID 10908tert-Butyl acetate溶媒

実験手順

A solution of 2-phenylacetic acid (12 g, 88 mmol) in tBuOAc (250 mL) in a 1 L round-bottomed flask was treated with perchloric acid, 70% redistilled (0.212 mL, 3.53 mmol), and stirred at room temperature for 20 hours. The solution was transferred very slowly to stirred mixture of saturated aqueous NaHCO3 and Et2O, which resulted in bubbling. The resulting layers were separated and the organic layer washed with saturated aqueous NaHCO3, dried over MgSO4, filtered, and concentrated to give tert-butyl 2-phenylacetate (11.6 g, 68% yield). 1H NMR (500 MHz, chloroform-d) δ 7.34-7.29 (m, 2H), 7.28-7.22 (m, 3H), 3.52 (s, 2H), 1.44 (s, 9H).

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. distillationredistilled (0.212 mL, 3.53 mmol)
  2. stirringto stirred
  3. additionmixture of saturated aqueous NaHCO3 and Et2O, which
  4. customresulted
  5. customin bubbling
  6. customThe resulting layers were separated
  7. washthe organic layer washed with saturated aqueous NaHCO3
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-4499a57caa764e0e80fc0895cd5edec7
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09133139B2

反応ノート

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