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Formic Acid → 4-Benzyl-2-(2-chloro-4-fluoro-phenyl)morpholine

HRID 880234
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HRID 880234 반응식
C(O)=O.[CH2:4]([NH:11][CH2:12][CH2:13]O)[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.Br[CH2:16][C:17]([C:19]1[CH:24]=[CH:23][C:22]([F:25])=[CH:21][C:20]=1[Cl:26])=[O:18]>C(Cl)Cl>[CH2:4]([N:11]1[CH2:12][CH2:13][O:18][CH:17]([C:19]2[CH:24]=[CH:23][C:22]([F:25])=[CH:21][C:20]=2[Cl:26])[CH2:16]1)[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 284Formic AcidHCID 4348BenzylethanolamineHCID 125933352-Chloro-4-fluorophenacyl bromide

생성물 1

HCID 897261154-Benzyl-2-(2-chloro-4-fluoro-phenyl)morpholine수율 99.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Combine formic acid (98-100%; 0.30 mL, 8 mmol) and 2-benzylaminoethanol (1.21 g, 8 mmol) and cool the resulting mixture with an ice bath. Add 2-bromo-1-(2-chloro-4-fluoro-phenyl)ethanone (1.0 g, 4 mmol); heat the mixture to reflux; and stir at that temperature for 20 h. Dilute the mixture with DCM and wash with saturated aqueous Na2CO3 solution. Dry organic phases over MgSO4; filter; collect the filtrate; and concentrate under reduced pressure. Purify via flash column chromatography eluting with a gradient of 0-20% methyl tertiary-butyl ether in hexanes. Combine the product fractions and remove the solvents under reduced pressure to give the title compound as a yellow oil (1.22 g, 43%). MS (m/z): 306 (M+1).

후처리

  1. temperatureheat the mixture
  2. temperatureto reflux
  3. washwash with saturated aqueous Na2CO3 solution
  4. filtrationfilter
  5. customcollect the filtrate
  6. concentrationand concentrate under reduced pressure
  7. customPurify via flash column chromatography
  8. washeluting with a gradient of 0-20% methyl tertiary-butyl ether in hexanes
  9. customCombine the product fractions and remove the solvents under reduced pressure

출처 및 근거

ORD 기록
ord-dcceaae92c9a49aa93eed45e0fab0345
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08993568B2

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