2-Tridecanone → 2,3-Dihydroperimidine

HRID 1936536

反応式

HRID 1936536 の反応式
[NH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[NH2:12])[CH:5]=[CH:4][CH:3]=1.[CH3:13]C(=O)CCCCCCCCCCC.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[NH:1]1[C:2]2=[C:11]3[C:6](=[CH:5][CH:4]=[CH:3]2)[CH:7]=[CH:8][CH:9]=[C:10]3[NH:12][CH2:13]1

参加物

5

実験手順

1,8-Diaminonaphthalene of 26.05 g, 32.66 g of 2-tridecanone, 55 mg of p-toluenesulfonic acid monohydrate, and 250 ml of toluene were mixed with stirring. The reaction mixture was refluxed with heating under a nitrogen atmosphere and was allowed to react for 5 hrs. using Dean-Stark trap to remove water from the reaction mixture Thereafter, the mixture was washed with aqueous saturated sodium hydrogen carbonate solution, dried using potassium carbonate anhydride, filtered and solvent was removed under reduced pressure. The product was distilled to obtain 46.50 g of dihydroperimidine intermediate, exhibiting a boiling point of 192 to 213° C./0.3 to 0.4 Torr. The thus prepared dihydroperimidine intermediate of 8.00 g, 1.48 g of squaric acid, 64 ml of n-butanol and 64 ml of toluene were mixed with stirring. The reaction mixture was refluxed with heating under a nitrogen atmosphere and was allowed to react for 3 hrs. using Dean-Stark trap to remove water from the reaction mixture Thereafter, the mixture was filtered, run into petroleum ether and allowed to stand at a temperature of 5° C. for 18 hrs. The product was filtered out, washed with petroleum ether and air-dried to obtain 6.00 g of squarylium dye SS-1. The dye was recrystalized from the mixture of tetrahydrofuran and petroleum ether to refine the product. exhibiting an maximum absorption wavelength (?max) of 802 nm (e=1.8×105) in ethyl acetate.

後処理

  1. temperatureThe reaction mixture was refluxed
  2. temperaturewith heating under a nitrogen atmosphere
  3. customto react for 5 hrs
  4. customusing Dean-Stark trap to remove water from the reaction mixture
  5. washthe mixture was washed with aqueous saturated sodium hydrogen carbonate solution
  6. customdried
  7. filtrationfiltered
  8. customsolvent was removed under reduced pressure
  9. distillationThe product was distilled

出典と根拠

ORDレコード
ord-a3aada3c236d41a791fd48dba5169359
出典データセット
uspto-grants-2002_05
特許番号
US06391535B1

関連ノート

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