Hydrochloric Acid → HCID 14555669、化合物
反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][C:11](=O)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=[O:18])=[CH:5][CH:4]=1.O.NN.Cl>C(O)COCCO.O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]([OH:19])=[O:18])=[CH:7][CH:8]=1参加物
実験手順
To a stirring solution of 7.5 gms 9(4-methoxyphenyl)-7-ketononanoic acid in 35 ml diethylene glycol was added 5.1 ml hydrazine hydrate. The mixture was heated to 120° for 4 hrs, cooled to room temperature, connected to a water aspirator, and gently heated to 120° to remove excess water and hydrazine. The reaction mixture was cooled to 70°, 7.2 gm KOH was added, and the mixture was heated up to 220° C. where it was kept for 5 hr, then cooled. The cooled reaction mass was dissolved in 120 ml hot water, acidified with conc. HCl, and 3× extracted with CHCl3. The combined organic phases were dried over MgSO4, filtered, and the solvent was evaporated in vacuo. Attempts to crystallize the product failed, so it was vacuum sublimed twice, dissolved in 300 ml chloroform, filtered through silica gel, and the solvent evaporated to give 38% product, a white solid of m.p. 41°-3° C.
後処理
- temperatureThe mixture was heated to 120° for 4 hrs
- temperaturegently heated to 120°
- customto remove excess water and hydrazine
- temperatureThe reaction mixture was cooled to 70°
- addition7.2 gm KOH was added
- temperaturethe mixture was heated up to 220° C. where it
- temperaturecooled
- customThe cooled reaction mass
- extractionextracted with CHCl3
- dry with materialThe combined organic phases were dried over MgSO4
- filtrationfiltered
- customthe solvent was evaporated in vacuo
- customto crystallize the product
- dissolutiondissolved in 300 ml chloroform
- filtrationfiltered through silica gel
- customthe solvent evaporated
出典と根拠
- ORDレコード
- ord-6c7c9aea9b8c407d906971b0fba53ff9
- 出典データセット
- uspto-grants-1989_08
- 特許番号
- US04861798
反応ノート
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