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Malic Acid → O-[4-(hexadecylamino)benzoyl]malic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Malic Acid | HCID 525 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | N-carbobenzyloxy-4-(hexadecylamino)benzoyl chloride | HCID 20437379 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | O-[4-(hexadecylamino)benzoyl]malic acid | HCID 86736912 | — |
反応手順
To a warm solution of N-carbobenzyloxy-4-(hexadecylamino)benzoyl chloride and 1.3 g. (1 eq) triethylamine in 100 ml. ether is treated with 2 g. (14.9 m moles) malic acid. An immediate precipitate forms, but the mixture is refluxed for one hour and filtered while hot. The solid is washed several times with hot ether, then the ether is evaporated to yield a white solid. The product is dissolved in tetrahydrofuran (100 ml.) and hydrogenated over 600 mg. 10% Pd(C) at 50 psi until hydrogen uptake stops. The catalyst is filtered, the solution is evaporated, and the residue is crystallized from acetic acid to yield the title compound as a tan, crystalline mass.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04196208 |
| 出典データセット | uspto-grants-1980_04 |
| ORD ID | ord-de465cf53f2b442588218722b46bc506 |
| 出典メモ | uspto-grants-1980_04 |