Diphenyl-o-tolylphosphine → [(2-Methylphenyl)diphenylphosphoranylidene]carbamic acid, ethyl ester
反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[P:8]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[C:21]([N:26]=[N+]=[N-])(=[O:25])[O:22][CH2:23][CH3:24]>CCOCC>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[P:8](=[N:26][C:21](=[O:25])[O:22][CH2:23][CH3:24])([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1参加物
4
実験手順
A solution of 1.0 g of (2-methylphenyl)diphenylphosphine in 30 ml of ether was treated with 4 ml of 1M ethyl carbonazidate in ether. The mixture was allowed to stand 48 hours, then repeatedly concentrated and finally treated with fresh ether and refrigerated, giving 930 mg of the desired compound, mp 113°-114° C.
後処理
- concentrationrepeatedly concentrated
- additionfinally treated with fresh ether
出典と根拠
- ORDレコード
- ord-073b4472a9e944b69d6799e1fda16a31
- 出典データセット
- uspto-grants-1990_01
- 特許番号
- US04894368
反応ノート
読み込み中…