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DL-alanine → 2-(Cyclopentylformamido)propanoic acid

HRID 11258
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HRID 11258 반응식
[NH2:1][CH:2]([C:4]([OH:6])=[O:5])[CH3:3].C(N(CC)CC)C.C[Si](Cl)(C)C.[CH:19]1([C:24](Cl)=[O:25])[CH2:23][CH2:22][CH2:21][CH2:20]1>ClCCl.O>[CH:19]1([C:24]([NH:1][CH:2]([CH3:3])[C:4]([OH:6])=[O:5])=[O:25])[CH2:23][CH2:22][CH2:21][CH2:20]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 602DL-alanineHCID 6397ChlorotrimethylsilaneHCID 8471TriethylamineHCID 78284Cyclopentanecarbonyl chloride

생성물 1

HCID 126219802-(Cyclopentylformamido)propanoic acid

시약·촉매·용매 2

HCID 962Water용매
HCID 6344
Dichloromethane
용매

실험 절차

16.8 g (0.189 mol) of D,L-alanine and 41.98 g (0.415 mol) of triethylamine are initially charged in 200 ml of dichloromethane. At 0° C. 45.07 g (0.415 mol) of trimethylsilyl chloride are added dropwise, and the mixture is stirred at room temperature for 1 h and then at 40° C. for 1 h. The solution is cooled to −10° C., and 25 g (0.189 mol) of cyclopentanecarbonyl chloride are added dropwise. The mixture is stirred at −10° C. for 2 h and at room temperature for 1 h. With ice-cooling, 100 ml of water are added dropwise, the mixture is stirred for 10 min. and the resulting precipitate is filtered off with suction. The precipitate is washed with 300 ml of water and then with 300 ml of diethyl ether and subsequently dried at 60° C.

후처리

  1. customAt 0° C
  2. waitat 40° C. for 1 h
  3. temperatureThe solution is cooled to −10° C.
  4. stirringThe mixture is stirred at −10° C. for 2 h and at room temperature for 1 h
  5. temperatureWith ice-cooling
  6. stirringthe mixture is stirred for 10 min.
  7. filtrationthe resulting precipitate is filtered off with suction
  8. washThe precipitate is washed with 300 ml of water
  9. dry with materialwith 300 ml of diethyl ether and subsequently dried at 60° C.

출처 및 근거

ORD 기록
ord-d94f79942acd4abda53fdab727364607
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07098207B2

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