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Trifluoroacetic acid → (S)-2-(2-Chloro-5-nitro-phenoxymethyl)-pyrrolidine

HRID 491592
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HRID 491592 반응식
C(OC([N:8]1[CH2:12][CH2:11][CH2:10][C@H:9]1[CH2:13][O:14][C:15]1[CH:20]=[C:19]([N+:21]([O-:23])=[O:22])[CH:18]=[CH:17][C:16]=1[Cl:24])=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[Cl:24][C:16]1[CH:17]=[CH:18][C:19]([N+:21]([O-:23])=[O:22])=[CH:20][C:15]=1[O:14][CH2:13][C@@H:9]1[CH2:10][CH2:11][CH2:12][NH:8]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 17755966HCID 17755966, 화합물

생성물 1

HCID 17755967(S)-2-(2-Chloro-5-nitro-phenoxymethyl)-pyrrolidine

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

(S)-2-(2-Chloro-5-nitro-phenoxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (6.94 g, 19.45 mmol) was stirred in 30 mL CH2Cl2 and 20 ml TFA for 3 h. The reaction was concentrated and dissolved in 0.1 N HCl (aq), which was basified to pH>12 with solid NaOH and extracted 3× with EtOAc. The organic layers were washed once with 1 N NaOH then once with a mixture of brine and 1 N NaOH. The organic layers were combined, dried over Na2SO4, filtered, and concentrated to dryness, to yield the title compound as a yellow solid.

후처리

  1. concentrationThe reaction was concentrated
  2. dissolutiondissolved in 0.1 N HCl (aq)
  3. extractionextracted 3× with EtOAc
  4. washThe organic layers were washed once with 1 N NaOH
  5. additiononce with a mixture of brine and 1 N NaOH
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-8174b9d4c373464b87a7f6dde7fe49a6
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07531553B2

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