反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=[O:10])=[CH:4][CH:3]=1.[CH2:12](Br)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].[OH-].[Na+]>[Cl-].C(C(CCCCCCCCCCCCCCCCCC)(CCCCCCCCCCCCCCCCCC)N)CCCCCCCCCCCCCCCCC.O>[CH2:25]([O:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([OH:11])=[O:10])=[CH:6][CH:7]=1)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH3:12]参加物
実験手順
A mixture of about 75 g of 4-hydroxyphenylacetic acid, about 273.38 g of 1-tetradecylbromide, about 46.33 g of sodium hydroxide, about 5.0 g of trioctadecyl methylamine chloride and about 500 ml of water was refluxed for about 24 hours with stirring, cooled to room temperature, the aqueous layer decanted and the solid washed with water. The solid was refluxed for about 2 hours with stirring in about 500 ml of ethanol containing about 40 g of sodium hydroxide and about 40 ml of water. The solvents were removed and the residue heated at about 0.1 mm and about 200°-210° C. in a Kugelrohr. The residue was stirred with dilute hydrochloric acid and ethyl acetate on a steam bath until solution was complete. The warm solution was washed with brine, then the solvent was removed and the residue recrystallized sequentially from methanol and hexane, giving about 66 g of the desired title compound as a white solid, mp 86°-87° C.
後処理
- temperaturewas refluxed for about 24 hours
- customthe aqueous layer decanted
- washthe solid washed with water
- temperatureThe solid was refluxed for about 2 hours
- stirringwith stirring in about 500 ml of ethanol containing about 40 g of sodium hydroxide and about 40 ml of water
- customThe solvents were removed
- temperaturethe residue heated at about 0.1 mm and about 200°-210° C. in a Kugelrohr
- stirringThe residue was stirred with dilute hydrochloric acid and ethyl acetate on a steam bath until solution
- washThe warm solution was washed with brine
- customthe solvent was removed
- customthe residue recrystallized sequentially from methanol and hexane
出典と根拠
- ORDレコード
- ord-da2ad265cd6e4817bd16622f17529c16
- 出典データセット
- uspto-grants-1987_02
- 特許番号
- US04640913
関連ノート
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