Hydrochloric Acid → 7-Methoxymethylbenzo-1,2,3-thiadiazole

HRID 257145

반응식

HRID 257145 반응식
[H-].[Na+].[OH:3][CH2:4][C:5]1[C:13]2[S:12][N:11]=[N:10][C:9]=2[CH:8]=[CH:7][CH:6]=1.[H][H].[CH3:16]I.Cl>CS(C)=O.O1CCCC1>[CH3:16][O:3][CH2:4][C:5]1[C:13]2[S:12][N:11]=[N:10][C:9]=2[CH:8]=[CH:7][CH:6]=1

참가 물질

8

반응물 5

HCID 313Hydrochloric AcidHCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 200964331,2,3-Benzothiadiazol-7-ylmethanolHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 200964277-Methoxymethylbenzo-1,2,3-thiadiazole

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 8028Tetrahydrofuran용매2회

실험 절차

1.4 g of sodium hydride (50% dispersion in oil) in 15 ml of absolute dimethyl sulfoxide are introduced into a reaction vessel, and a solution of 4.15 g of 7-hydroxymethylbenzo-1,2,3-thiadiazole in 15 ml of tetrahydrofuran is added dropwise at 0°-5° C. under a nitrogen atmosphere and with stirring, during which process hydrogen is evolved. After 20 minutes of stirring at 10° C., the mixture is cooled down to 0°-5° C., and a solution of 4 g of methyl iodide in 15 ml of tetrahydrofuran is added dropwise. Stirring is continued for another hour at room temperature, and the mixture is cooled, treated with ice-water, neutralised with dilute hydrochloric acid and extracted with ethyl acetate. The extracts are washed with water, dried over sodium sulfate and evaporated, and the residue is dried in a high vacuum, resulting in the title compound in the form of a yellow oil, nD27 =1.5912.

후처리

  1. stirringAfter 20 minutes of stirring at 10° C.
  2. temperaturethe mixture is cooled down to 0°-5° C.
  3. stirringStirring
  4. waitis continued for another hour at room temperature
  5. temperaturethe mixture is cooled
  6. extractionextracted with ethyl acetate
  7. washThe extracts are washed with water
  8. dry with materialdried over sodium sulfate
  9. customevaporated
  10. customthe residue is dried in a high vacuum

출처 및 근거

ORD 기록
ord-573aec29607b4d85b5e99041ece57b30
출처 데이터셋
uspto-grants-1993_11
특허 번호
US05260423

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