Dimethyl Sulfoxide → 2-(4-Methoxyphenyl)oxirane

HRID 596612

반응식

HRID 596612 반응식
[H-].[Na+].CS(C)=O.[I-].[CH3:8][S+](C)C.[CH3:12][O:13][C:14]1[CH:21]=[CH:20][C:17]([CH:18]=[O:19])=[CH:16][CH:15]=1>O.O1CCCC1>[CH3:12][O:13][C:14]1[CH:21]=[CH:20][C:17]([CH:18]2[O:19][CH2:8]2)=[CH:16][CH:15]=1

참가 물질

7

반응물 4

HCID 679Dimethyl SulfoxideHCID 24758Sodium hydrideHCID 312444-MethoxybenzaldehydeHCID 75127Trimethylsulfonium iodide

생성물 1

HCID 980482-(4-Methoxyphenyl)oxirane

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
-5 °C

실험 절차

A suspension of 4.84 g. of sodium hydride (57% mineral oil dispersion) in 70 ml. of dry dimethyl sulfoxide is heated at about 65° C. under argon with stirring for 1 hour. Dry tetrahydrofuran (75 ml.) is added and the resulting solution is cooled to -5° C. Trimethylsulfonium iodide (19 g., 92.8 mmol) is added very slowly and stirring is continued for about 5 minutes. A solution of 12.6 g. (92.8 mmol) of p-methoxybenzaldehyde in 120 ml. of tetrahydrofuran is added and the temperature is maintained at -5° C. After addition is completed the mixture is allowed to warm to room temperature, poured into water and extracted with ether. The extract is washed with saturated sodium chloride solution, dried and evaporated to give p-methoxystyrene oxide.

후처리

  1. additionA suspension of 4.84 g
  2. stirringstirring
  3. waitis continued for about 5 minutes
  4. temperaturethe temperature is maintained at -5° C
  5. additionAfter addition
  6. temperatureto warm to room temperature
  7. extractionextracted with ether
  8. washThe extract is washed with saturated sodium chloride solution
  9. customdried
  10. customevaporated

출처 및 근거

ORD 기록
ord-4da0328f32a445f8b0a12e1ec02d976a
출처 데이터셋
uspto-grants-1977_03
특허 번호
US04011319

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