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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → HCID 68533409, 화합물

HRID 1808232
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HRID 1808232 반응식
C(OC(=O)[NH:7][CH:8]1[CH2:13][CH:12]2[CH2:14][CH2:15][CH:9]1[CH2:10][C:11]2=[O:16])(C)(C)C.[C:18]([OH:24])([C:20]([F:23])([F:22])[F:21])=[O:19]>C(Cl)Cl>[F:21][C:20]([F:23])([F:22])[C:18]([OH:24])=[O:19].[NH2:7][CH:8]1[CH2:13][CH:12]2[CH2:14][CH2:15][CH:9]1[CH2:10][C:11]2=[O:16]
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 68535128HCID 68535128, 화합물

생성물 1

HCID 68533409HCID 68533409, 화합물수율 92%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

(5-Oxo-bicyclo[2.2.2]oct-2-yl)-carbamic acid tert-butyl ester (Preparation 75, 279 g, 1.17 mol, 10 eq) was taken up in DCM (450 mL). TFA (416 mL, 5.60 mol, 4.8 eq) was added dropwise. On addition, the reaction warms to reflux while much gas evolves. The reaction mixture was kept at reflux temperature for 1 hour after which it was allowed to cool to room temperature overnight. The mixture was concentrated and the residue was taken up in DCM (50 mL) and then tert-butyl methyl ether (1.3 L) was added which resulted in a brown suspension. The solids were collected by filtration (P3) and were washed with tert-butyl methyl ether. The latter was dried in vacuo (40° C.) to furnish title compound as an off-white solid (272 g, 1.07 mol, 92%).

후처리

  1. additionOn addition
  2. temperatureto reflux while much gas evolves
  3. temperatureat reflux temperature for 1 hour after which it
  4. concentrationThe mixture was concentrated
  5. additiontert-butyl methyl ether (1.3 L) was added which
  6. customresulted in a brown suspension
  7. filtrationThe solids were collected by filtration (P3)
  8. washwere washed with tert-butyl methyl ether
  9. customThe latter was dried in vacuo (40° C.)

출처 및 근거

ORD 기록
ord-fa6f5713749841be811f0b77d36ec527
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08357711B2

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