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HRID 36134作成日:2026年10月25日
2,4,6-Trimethylpyridine → (R)-3-Carboxy-N,N,N-trimethyl-2-{[hydroxy(tetradecyloxy)phosphinyl]oxy}-1-propanaminium Hydroxide
https://huagongshe.com/reaction/36134
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| 反応物 | (-)-Carnitine | HCID 10917 | — |
| 反応物 | Tetrafluoroborate | HCID 26255 | — |
| 反応物 | Sodium periodate | HCID 23667635 | — |
| 反応物 | Dichlorotetradecylphosphite | HCID 86748667 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (R)-3-Carboxy-N,N,N-trimethyl-2-{[hydroxy(tetradecyloxy)phosphinyl]oxy}-1-propanaminium Hydroxide | HCID 86748666 | — |
反応手順
To a solution of 16.4 gm of the tetrafluoroborate salt of L-carnitine and 26 gm of collidine in 263 ml of acetonitrile is added 29.4 gm of dichlorotetradecylphosphite. The reaction mixture is stirred at room temperature for 17 hours and then a solution of 21.1 gm of sodium metaperiodate in 48.7 ml of water is added. After stirring at room temperature for two hours, the reaction mixture is filtered through Celite and the filtrate is concentrated under vacuum. The residue is flash chromatographed on normal phase silica gel, initially with a 50/30/3 ratio of chloroform/methanol/concentrated ammonium hydroxide and then with a 50/30/10 ratio of the same solvent system to yield a product that is then flash chromatographed on LiChroprep RP-8 silica gel using gradients from water to acetonitrile and to methanol. The title compound is isolated as an amorphous solid, (m.p. ~190° C. [dec]; 31P NMR=0.324 ppm; [α]25 =-10.34 C=1.0 MeOH).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05412137 |
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| 出典データセット | uspto-grants-1995_05 |
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| ORD ID | ord-f07963c8584147a5b1e3af067d4981b6 |
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| 出典メモ | uspto-grants-1995_05 |
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