Chloroacetonitrile → 5-tert-Butyl-2-(chloromethyl)-1,3-oxazole

HRID 1385194노트

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HRID 1385194 반응식
B(F)(F)F.CCOCC.[N+:10](=[CH:12][C:13](=[O:18])[C:14]([CH3:17])([CH3:16])[CH3:15])=[N-].C(=O)(O)[O-].[Na+].[Cl:24][CH2:25][C:26]#N>>[Cl:24][CH2:25][C:26]1[O:18][C:13]([C:14]([CH3:17])([CH3:16])[CH3:15])=[CH:12][N:10]=1

참가 물질

5

반응물 4

HCID 7856Chloroacetonitrile2회HCID 8000Boron trifluoride etherateHCID 516892Sodium BicarbonateHCID 217927841-Diazonio-3,3-dimethylbut-1-en-2-olate

생성물 1

HCID 129689745-tert-Butyl-2-(chloromethyl)-1,3-oxazole

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온도
0 °C

실험 절차

To a solution of 2 mL (2.3 g, 16 mmol) of boron trifluoride etherate in 20 mL of chloroacetonitrile at 0° C. was added a solution of 1.33 g (10 mmol) of 1-diazo-3,3-dimethyl-2-butanone in 5 mL of chloroacetonitrile dropwise. The resulting solution was stirred at 0° C. for 0.5 h. The reaction mixture was added to saturated aqueous sodium bicarbonate solution to neutralize the acid and the product was extracted three times with dichloromethane. The combined extracts was dried (sodium sulfate), concentrated and purified by flash column chromatography (Merck silica, 25×200 mm, dichloromethane) to give 1.1 g of 2-(chloromethyl)-5-t-butyloxazole as a yellow liquid (6.4 mmol, 64% overall from the acid chloride).

후처리

  1. extractionthe product was extracted three times with dichloromethane
  2. dry with materialThe combined extracts was dried (sodium sulfate)
  3. concentrationconcentrated
  4. custompurified by flash column chromatography (Merck silica, 25×200 mm, dichloromethane)

출처 및 근거

ORD 기록
ord-65bc07e5a21343ce831b411f55b81294
출처 데이터셋
uspto-grants-2001_07
특허 번호
US06262096B1

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