Tetramethylammonium fluoride → Tert-butyl 3-(5-chloro-2-hydroxyphenyl)azetidine-1-carboxylate

HRID 1692274

반응식

HRID 1692274 반응식
[Si]([O:8][C:9]1[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:10]=1[CH:16]1[CH2:19][N:18]([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:17]1)(C(C)(C)C)(C)C.[F-].C[N+](C)(C)C>O1CCCC1>[Cl:15][C:12]1[CH:13]=[CH:14][C:9]([OH:8])=[C:10]([CH:16]2[CH2:17][N:18]([C:20]([O:22][C:23]([CH3:25])([CH3:24])[CH3:26])=[O:21])[CH2:19]2)[CH:11]=1

참가 물질

4

실험 절차

To a solution of tert-Butyl 3-(2-{[tert-butyl(dimethyl)silyl]oxy}-5-chlorophenyl)azetidine-1-carboxylate (Preparation 238, 3.1 g, 7.79 mmol) in tetrahydrofuran (80 ml) was added tetramethylammonium fluoride (1.0 g, 10.74 mmol). The mixture was stirred at room temperature for 18 hours before concentrating in vacuo. The residue was partitioned between tert-butyl methyl ether (100 ml) and aqueous sodium hydroxide solution. The organics were dried over sodium sulfate, filtered and evaporated in vacuo to give a reddish brown oil, 2.33 g. This was purified by column chromatography (100 g of silica) eluting with heptane:ethyl acetate (6:4, by volume) to afford the title compound as a reddish brown gum, 850 mg, 38% yield.

후처리

  1. concentrationbefore concentrating in vacuo
  2. customThe residue was partitioned between tert-butyl methyl ether (100 ml) and aqueous sodium hydroxide solution
  3. dry with materialThe organics were dried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated in vacuo
  6. customto give a reddish brown oil, 2.33 g
  7. customThis was purified by column chromatography (100 g of silica)
  8. washeluting with heptane:ethyl acetate (6:4, by volume)

출처 및 근거

ORD 기록
ord-06238cd149fa435eb08dc2e15e1aa44e
출처 데이터셋
uspto-grants-2012_04
특허 번호
US08153814B2

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