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HRID 268043作成日:2026年10月25日

Thionyl Chloride → HCID 68134844、化合物

https://huagongshe.com/reaction/268043

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物3-(Diethylamino)-2,2-dimethylpropan-1-olHCID 295965—
反応物4-Chlorocinnamic acidHCID 637797—
溶媒BenzeneHCID 241—
生成物HCID 68134844HCID 68134844—

反応手順

P-Chlorocinnamic acid (27.5 g, 0.15 mole) was added with rapid stirring to thionyl chloride (52.5 ml) and refluxed for 31/2 hours. The mixture was stripped of excess thionyl chloride under reduced pressure, benzene (100 ml) was added and the mixture was again stripped of solvent. The residue was treated with a solution of 3-diethylamino-2,2-dimethylpropanol (24.2 g, 0.15 mole) in benzene (500 ml), refluxed for 3 hours, cooled, diluted with petroleum ether (500 ml), and stored overnight at room temperature. The benzene-petroleum ether solution was decanted, the residue dissolved in H2O (700 ml) and the solution adjusted to pH 10 with saturated aqueous K2CO3 (60 ml). The product was extracted from the aqueous phase with benzene (800 ml) in portions and the extract dried overnight over MgSO4 and Darco. The solution was filtered and the filtrate adjusted to pH 2 with a solution of dry HCl in ether (cooled in an ice bath). Petroleum ether (500 ml) was added and the product oiled out of solution. The benzene-petroleum ether solution was decanted and the product was recrystallized from ethyl acetate (600 ml), yield: 33 g (61%). A sample was recrystallized from ethyl acetate, m.p. 132°-134°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03946042
出典データセットuspto-grants-1976_03
ORD IDord-c97a9d536b1449da98bcfd645ef1d0af
出典メモuspto-grants-1976_03