Tetrahydrofuran → Trifluoroacetic acid

HRID 2111529노트

반응식

HRID 2111529 반응식
[CH:1]([N:14]1[CH2:17][C:16](=[O:18])[CH2:15]1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:19][C:20]([Si](C)(C)C)([F:22])[F:21].[F-].[Cs+].C1[CH2:33][O:32]CC1>>[CH:1]([N:14]1[CH2:17][C:16]([C:20]([F:22])([F:21])[F:19])([OH:18])[CH2:15]1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1.[C:33]([OH:32])([C:20]([F:22])([F:21])[F:19])=[O:18]

참가 물질

6

실험 절차

To a solution of 1-benzhydryl-azetidin-3-one (400 mg, 1.69 mmol) in THF (5 mL), trifluoromethyltrimethylsilane (360 mg, 2.53 mmol) and cesium fluoride(390 mg, 2.57 mmol) were added. The reaction mixture was stirred at rt. for 1 hr. Then it was quenched with 5 mL saturated NH4Cl solution and tetrabutylammonium fluoride (200 mg) was added. The resulting reaction mixture was stirred at rt. for three days. It was then extracted with ether (3×20 mL). The organic layers were combined, dried (MgSO4) and concentrated to give an orange oil as crude product. It was then purified by Prep.HPLC column to afford a white solid as final product as TFA salt. (350 mg, 49% yield). Retention time: 1.442 min. 1H NMR (500 MHz, MeOD) δ ppm 3.92 (d, J=11.29 Hz, 2 H) 4.35 (d, J=11.60 Hz, 2 H) 5.44 (s, 1 H) 7.34-7.55 (m, 10 H).

후처리

  1. customThen it was quenched with 5 mL saturated NH4Cl solution and tetrabutylammonium fluoride (200 mg)
  2. additionwas added
  3. customThe resulting reaction mixture
  4. stirringwas stirred at rt
  5. waitfor three days
  6. extractionIt was then extracted with ether (3×20 mL)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated
  9. customto give an orange oil as crude product
  10. customIt was then purified by Prep.HPLC column

출처 및 근거

ORD 기록
ord-95f23482c76e47a4a6fa5bdd54386fba
출처 데이터셋
uspto-grants-2009_04
특허 번호
US07521442B2

반응 노트

불러오는 중…