Sodium Sulfate → 3,5-Dimethyl-4-(hydroxymethyl)isoxazole

HRID 442023

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HRID 442023 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[C:7]([C:12]1[C:13]([CH3:18])=[N:14][O:15][C:16]=1[CH3:17])(OCC)=[O:8].S([O-])([O-])(=O)=O.[Na+].[Na+]>CCOCC>[CH3:18][C:13]1[C:12]([CH2:7][OH:8])=[C:16]([CH3:17])[O:15][N:14]=1

참가 물질

5

실험 절차

A suspension of 100 g. (2.63 moles) of lithium aluminum hydride in 2.5 liters of anhydrous ether was stirred under nitrogen as a solution of 272 g. (1.61 mole) of the 4-carboethoxy-3,5-dimethylisoxazole prepared in Example 1 above in 400 ml. of anhydrous ether was added at such a rate as to maintain a gentle reflux. The suspension was stirred at room temperature under nitrogen overnight, during which time an extremely gummy green-gray mass formed in the bottom of the flask. The mixture was cooled in an ice bath and hydrolyzed with saturated aqueous sodium sulfate solution. Anhydrous sodium sulfate was added to dry the ether solution. The salts were removed by filtration and washed carefully with ether and chloroform. Solvent removal from the filtrates, finally at 50°/0.1 mm., gave a white crystalline mass. This was triturated with hot ether and then cooled. Filtration gave 3,5-dimethyl-4-hydroxymethyl-isoxazole as white prisms, m.p. 76.5°-77.5°. Concentration of the mother liquors gave a second crop of prisms, m.p. 76.5°-78°.

후처리

  1. additionA suspension of 100 g
  2. temperatureto maintain a gentle reflux
  3. customformed in the bottom of the flask
  4. dry with materialto dry the ether solution
  5. customThe salts were removed by filtration
  6. washwashed carefully with ether and chloroform
  7. customSolvent removal from the filtrates
  8. customfinally at 50°
  9. custom, gave a white crystalline mass
  10. customThis was triturated with hot ether
  11. temperaturecooled
  12. filtrationFiltration

출처 및 근거

ORD 기록
ord-c9b4ad6a2efd4e94804cebff9296db1e
출처 데이터셋
uspto-grants-1977_08
특허 번호
US04044004

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