Cyclopentylamine → Tert-butyl 2-(cyclopentylamino)acetate

HRID 127625노트

반응식

HRID 127625 반응식
[CH:1]1([NH2:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.C(N(CC)CC)C.Br[CH2:15][C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17]>CCOCC>[C:19]([O:18][C:16](=[O:17])[CH2:15][NH:6][CH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1)([CH3:22])([CH3:21])[CH3:20]

참가 물질

5

반응물 3

HCID 2906CyclopentylamineHCID 8471TriethylamineHCID 79177tert-Butyl bromoacetate

생성물 1

HCID 13298943Tert-butyl 2-(cyclopentylamino)acetate수율 66%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a chilled (0°-5° C.) and stirred ethereal solution (500 ml) containing cyclopentyl amine (75 g, 0.88 mol) and triethyl amine (101 g, 1.0 mol) was added t-butyl bromoacetate (136.5 g, 0.7 mol) in ether (300 ml). The reaction mixture was stirred overnight. The ethereal mixture was then concentrated and the residue redissolved in methylene chloride (750 ml). This solution was washed with saturated aqueous sodium bicarbonate (1000 ml), water (2×3000 ml), and brine (2000 ml). The organic portion was separated, dried over MgSO4, filtered and evaporated yielding N-cyclopentylglycine t-butyl ester (92 g, 66%) as a brown oil which slowly crystallized on standing.

후처리

  1. temperatureTo a chilled (0°-5° C.)
  2. concentrationThe ethereal mixture was then concentrated
  3. dissolutionthe residue redissolved in methylene chloride (750 ml)
  4. washThis solution was washed with saturated aqueous sodium bicarbonate (1000 ml), water (2×3000 ml), and brine (2000 ml)
  5. customThe organic portion was separated
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customevaporated

출처 및 근거

ORD 기록
ord-19059f66fe404d81bba0e4a7822a2b75
출처 데이터셋
uspto-grants-1981_03
특허 번호
US04256761

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