反応式
[C:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([CH3:14])([CH3:13])[CH2:8][CH2:7][C:6]2([CH3:16])[CH3:15])#[CH:2].[CH:17]([C:19]1[CH:28]=[CH:27][C:22]([C:23]([O:25][CH3:26])=[O:24])=[CH:21][CH:20]=1)=O.[NH2:29][C:30]([NH2:32])=[O:31].S(=O)(=O)(O)O.[CH2:38](O)[CH2:39][CH2:40]C>CCOCC.O>[C:23]([C:22]1[CH:27]=[CH:28][C:19]([C:17]2[CH:2]=[C:1]([C:3]3[CH:12]=[CH:11][C:10]4[C:9]([CH3:14])([CH3:13])[CH2:8][CH2:7][C:6]([CH3:16])([CH3:15])[C:5]=4[CH:4]=3)[N:32]=[C:30]([OH:31])[N:29]=2)=[CH:20][CH:21]=1)([O:25][CH2:26][CH2:38][CH2:39][CH3:40])=[O:24]参加物
8
実験手順
21 g (0.1 mole) of 6-ethynyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene, 16 g (0.1 mole) of methyl 4-formylbenzoate, 9 g (0.15 mole) of urea and 15 ml of concentrated sulfuric acid in 50 ml of n-butanol were refluxed for 4 hours. After cooling, the mixture was poured onto 500 ml of water, 100 ml of ether were added and stirring was carried out for 5 minutes. A solid was precipitated between phases. In a shaking funnel, the aqueous phase was separated off and the residue was again washed with water and then shaken thoroughly with 200 ml of petroleum ether. The precipitate was filtered off under suction and washed with petroleum ether. 6.5 g of the title compound of melting point 267°-277° C. were obtained in this manner.
後処理
- temperatureAfter cooling
- additionwere added
- customA solid was precipitated between phases
- customIn a shaking funnel, the aqueous phase was separated off
- washthe residue was again washed with water
- stirringshaken thoroughly with 200 ml of petroleum ether
- filtrationThe precipitate was filtered off under suction
- washwashed with petroleum ether
出典と根拠
- ORDレコード
- ord-5db870c3a531410889b630b942b2bf38
- 出典データセット
- uspto-grants-1991_10
- 特許番号
- US05061705
関連ノート
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