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Phenylacetic Acid → Tert-butyl 2-phenylacetate

HRID 1771952
ノート
印刷プレビュー

反応式

HRID 1771952 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 68%

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) stirred at room temperature for 20 hours. The solution was transferred very slowly to stirred mixture of saturated aqueous NaHCO3 and Et2O. Extensive bubbling was observed. 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, Intermediate S5A (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).

後処理

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

出典と根拠

ORDレコード
ord-a13b233684f34c0c9b69195d5f126035
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09249157B2

反応ノート

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