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Toluene → 2-Stearamidoethyl 3,4-di-tert-butyl-4-hydroxybenzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | 3,5-Di-tert-butyl-4-hydroxybenzoic acid | HCID 15007 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | N-Stearoylethanolamine | HCID 27902 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 2-Stearamidoethyl 3,4-di-tert-butyl-4-hydroxybenzoate | HCID 70565995 | — |
反応手順
A mixture of 25 g (0.1 mole) 3,5-di-tert-butyl-4-hydroxybenzoic acid, 50 ml toluene and 8.5 ml thionyl chloride was refluxed for 3 hours. The excess thionyl chloride and the toluene were removed on a rotary evaporator. The acid chloride was dissolved in 50 ml toluene and was added to a mixture of 29.4 g (0.09 mole) N-(2-hydroxyethyl)stearamide, 20 ml toluene and 15 ml pyridine. The mixture was refluxed for two hours. The reaction mixture was then cooled, quenched with water, washed with dilute hydrochloric acid and with water. The toluene was removed by distillation, and the residue was crystallized from hexane. The title compound thus obtained melted at 56°-58° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04305868 |
| 出典データセット | uspto-grants-1981_12 |
| ORD ID | ord-e04349d6adcb43a9bd7514c7e121c661 |
| 出典メモ | uspto-grants-1981_12 |