1-Butanol → HCID 178450655、化合物

HRID 346292

反応式

HRID 346292 の反応式
[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

  1. temperatureAfter cooling
  2. additionwere added
  3. customA solid was precipitated between phases
  4. customIn a shaking funnel, the aqueous phase was separated off
  5. washthe residue was again washed with water
  6. stirringshaken thoroughly with 200 ml of petroleum ether
  7. filtrationThe precipitate was filtered off under suction
  8. 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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