Ethyl cyanoformate → ethyl 1-(4-methoxybenzyl)-1H-tetrazole-5-carboxylate
反応式
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]([CH2:7][N:8]=[N+:9]=[N-:10])=[CH:5][CH:4]=1.[C:13]([C:15]([O:17][CH2:18][CH3:19])=[O:16])#[N:14]>C1(C)C(C)=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][N:8]2[C:13]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[N:14][N:10]=[N:9]2)=[CH:11][CH:12]=1参加物
4
実験手順
A mixture of crude 4-methoxybenzyl azide (45.3 g; prepared as described below) and ethyl cyanoformate (33 g) in xylene (300 ml) was heated at reflux for 48 hours. The mixture was evaporated at below 40° C. and under reduced pressure to leave a residue of ethyl 1-(4-methoxybenzyl)-1H-tetrazole-5-carboxylate (69.36 g), m.p. 52° C.
後処理
- temperaturewas heated
- temperatureat reflux for 48 hours
- customThe mixture was evaporated at below 40° C. and under reduced pressure
出典と根拠
- ORDレコード
- ord-37265387fae74eff98b258c00dbba15b
- 出典データセット
- uspto-grants-1984_04
- 特許番号
- US04442115
反応ノート
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