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Methyl iodide → 3,6-Dimethoxyphthalonitrile

HRID 437982
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HRID 437982 반응식
[C:1]([C:3]1[C:9]([C:10]#[N:11])=[C:8]([OH:12])[CH:7]=[CH:6][C:4]=1O)#[N:2].[CH3:13]I.[C:15](=[O:18])([O-])[O-].[K+].[K+]>O>[CH3:13][O:12][C:8]1[CH:7]=[CH:6][C:4]([O:18][CH3:15])=[C:3]([C:1]#[N:2])[C:9]=1[C:10]#[N:11]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 784672,3-Dicyanohydroquinone

생성물 1

HCID 3583583,6-Dimethoxyphthalonitrile

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 17.1 g. of 2,3-dicyanohydroquinone, 143.5 g. of methyl iodide and 43.5 g. of potassium carbonate is stirred in dimethylformide for approximately 20 hours. The mixture is then treated with 1 liter of water and filtered. The precipitate is washed with water and methanol and dried to yield 3,6-dimethoxyphthalonitrile. The nitrile is then slurried in 150 ml. of sodium hydroxide and heated at 115° C. for approximately seven hours. The resulting solution is cooled, filtered and acidified with hydrochloric acid to precipitate 3,6-dimethoxyphthalic acid. The acid is refluxed in 150 ml. of acetic anhydride for 15 hours and then cooled to room temperature. The resulting crystals are filtered and washed with ether to yield 3,6-dimethoxyphthalic anhydride having a melting point of 265°-268° C.

후처리

  1. additionA mixture of 17.1 g
  2. filtrationfiltered
  3. washThe precipitate is washed with water and methanol
  4. customdried

출처 및 근거

ORD 기록
ord-12fe172da7a4455d90d76d7a3bbe0a7b
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04032656

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