Cyclopentylamine → Methyl 2-(cyclopentylamino)acetate

HRID 875970ノート

反応式

HRID 875970 の反応式
Br[CH2:2][C:3]([O:5][CH3:6])=[O:4].[CH:7]1([NH2:12])[CH2:11][CH2:10][CH2:9][CH2:8]1.C(N(CC)CC)C>C1COCC1>[CH:7]1([NH:12][CH2:2][C:3]([O:5][CH3:6])=[O:4])[CH2:11][CH2:10][CH2:9][CH2:8]1

参加物

5

実験手順

A solution of methyl bromoacetate (17.4 mL, 188 mmol) in THF (40 mL) was dropwise added to a solution of cyclopentylamine (18.6 mL, 188 mmol) and triethylamine (26.1 mL, 188 mmol) in THF (150 mL) at 0° C. Following addition, the reaction was allowed to reach room temperature and was stirred overnight. The triethylammonium salts were filtered and rinsed with scant THF. The combined filtrates were concentrated in vacuo. The desired product was distilled from the residuals under reduced pressure to yield 20.2 g of compound 225 (68% yield). 1H NMR (500 MHz, CDCl3) δ ppm 3.73 (s, 3 H) 3.41 (s, 2 H) 3.00-3.13 (m, J=12.90, 6.39, 6.39 Hz, 1 H) 1.77-1.87 (m, 2 H) 1.67-1.74 (m, 2 H) 1.48-1.59 (m, 2 H) 1.29-1.41 (m, 2 H) ppm.

後処理

  1. additionaddition
  2. customto reach room temperature
  3. filtrationThe triethylammonium salts were filtered
  4. washrinsed with scant THF
  5. concentrationThe combined filtrates were concentrated in vacuo
  6. distillationThe desired product was distilled from the residuals under reduced pressure

出典と根拠

ORDレコード
ord-f2c661aaac314ec983aeea249a9399cd
出典データセット
uspto-grants-2015_03
特許番号
US08980903B2

反応ノート

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