(Diethylamino)sulfur trifluoride → Tert-butyl (2-fluoro-2-methylpropyl)carbamate

HRID 1798878노트

반응식

HRID 1798878 반응식
O[C:2]([CH3:13])([CH3:12])[CH2:3][NH:4][C:5](=[O:11])[O:6][C:7]([CH3:10])([CH3:9])[CH3:8].C(N(S(F)(F)[F:20])CC)C.C([O-])(O)=O.[Na+]>C(Cl)Cl>[F:20][C:2]([CH3:13])([CH3:12])[CH2:3][NH:4][C:5](=[O:11])[O:6][C:7]([CH3:10])([CH3:9])[CH3:8]

참가 물질

5

반응물 3

HCID 123472(Diethylamino)sulfur trifluorideHCID 516892Sodium BicarbonateHCID 11106129tert-Butyl 2-hydroxy-2-methylpropylcarbamate

생성물 1

HCID 72698934Tert-butyl (2-fluoro-2-methylpropyl)carbamate수율 79.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
-78 °C

실험 절차

A stirred solution of tert-butyl 2-hydroxy-2-methylpropylcarbamate (7.81 g, 41.3 mmol) dissolved in 300 mL of anhydrous CH2Cl2 was cooled to −78° C. under an atmosphere of N2. The reaction mixture was treated with diethylaminosulfur trifluoride (DAST) (6.2 mL, 47 mmol) and allowed to warm to ambient temperature overnight. The reaction mixture was treated with saturated NaHCO3 solution and the layers were separated. The organic portion was washed successively with saturated NaHCO3 solution, H2O and brine. The organic portion was dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% EtOAc/hexanes) gave 6.27 g of tert-butyl 2-fluoro-2-methylpropylcarbamate as an amber oil which solidified on standing.

후처리

  1. temperatureto warm to ambient temperature overnight
  2. customthe layers were separated
  3. washThe organic portion was washed successively with saturated NaHCO3 solution, H2O and brine
  4. dry with materialThe organic portion was dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-30e806c3fedf446f8086d9bb66409e1c
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08343993B2

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