Hydrochloric Acid → 2-(Hydroxyimino)-5,6-dimethoxy-2,3-dihydro-1H-inden-1-one
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[C:8](=[O:14])[CH2:7][CH2:6]2.[N:15](OCCC(C)C)=[O:16].Cl>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[C:8](=[O:14])[C:7](=[N:15][OH:16])[CH2:6]2参加物
5
実験手順
5,6-Dimethoxy-1-indanone (0.078 moles, 15 g) is dissolved in absolute ethanol (550 ml), thermostated at 50° C., and added with isoamyl nitrite (0.086 moles, 11.9 ml) and conc. HCl (11.9 ml). After a few minutes the product precipitates. The reaction is kept at 50° C. for further 3 hours, then cooled at r.t. and the solid is filtered washing with absolute ethanol (50 ml) and ethyl ether (100 ml). The product is dried in oven under vacuum at r.t. Yield: 16.3 g (94.4%)
後処理
- customAfter a few minutes the product precipitates
- filtrationthe solid is filtered
- washwashing with absolute ethanol (50 ml) and ethyl ether (100 ml)
- customThe product is dried in oven under vacuum at r.t
出典と根拠
- ORDレコード
- ord-d936209124fc4f798932fc5b440e1bda
- 出典データセット
- uspto-grants-2000_09
- 特許番号
- US06114391
反応ノート
読み込み中…