Ethylene Glycol → 3',4'-Dihydro-2'-(1H-1,2,4-Triazol-1-yl)-Spiro-[1,3-Dioxolane-2,1'(2'H)-Naphthalene]
反応式
[N:1]1([CH:6]2[CH2:15][CH2:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7]2=[O:16])[CH:5]=[N:4][CH:3]=[N:2]1.[CH2:17](O)[CH2:18][OH:19].C1(C)C=CC(S(O)(=O)=O)=CC=1.C1(C)C=CC=CC=1>ClCCl.C(O)CCC>[N:1]1([CH:6]2[CH2:15][CH2:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7]32[O:19][CH2:18][CH2:17][O:16]3)[CH:5]=[N:4][CH:3]=[N:2]1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A mixture of 10 g. 3,4-dihydro-2-(1H-1,2,4-triazol-1-yl)-1-(2H)-naphthalenone, 5.8 g. ethylene glycol and 11.5 g. p-toluenesulfonic acid was refluxed in a mixed solvent of 150 ml. toluene and 70 ml. n-butanol under a Dean-Stark [trademark] trap for 48 hours. The solvent was evaporated leaving a slurry which was taken up in dichloromethane and washed twice with 10% aqueous sodium hydroxide and once with water. The extract was dried in sodium sulfate, filtered and evaporated leaving an oily residue which crystallized on cooling to yield 1.5 g. of white crystals. These white crystals were 3',4'-dihydro-2'-(1H-1,2,4-triazole-1-yl)-spiro-[1,3-dioxolane-2,1'(2'H)-naphthalene. This compound had a melting point of 108° C.
後処理
- additionA mixture of 10 g
- customThe solvent was evaporated
- customleaving a slurry which
- washwashed twice with 10% aqueous sodium hydroxide and once with water
- dry with materialThe extract was dried in sodium sulfate
- filtrationfiltered
- customevaporated
- customleaving an oily residue which
- customcrystallized
- temperatureon cooling
- customto yield 1.5 g
出典と根拠
- ORDレコード
- ord-48027628fa7447ea9860ebb15c41398f
- 出典データセット
- uspto-grants-1990_07
- 特許番号
- US04943311
反応ノート
読み込み中…