関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | L-Hydroxyproline | HCID 5810 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 生成物 | 4-Hydroxy-L-proline methyl ester hydrochloride | HCID 11435319 | — |
反応手順
To a suspension of trans-4-hydroxy-L-proline (100 g, 0.76 mol, 1 equivalent) in methanol (850 mL), thionyl chloride (110 mL, 1.53 mol, 2 equivalents) was added drop-wise at 0-5° C. Then the reaction mixture was stirred for 4 hours at 20-25° C. The reaction mixture was concentrated under reduced pressure. The crude material was stirred in a mixture of ethanol-methyl tert-butyl ether (1:4, 500 mL) for 30 minutes and the solid was collected by filtration. The wet cake was dried in a vacuum tray dryer for 8 hours at about 50° C. to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 2.09-2.24 (m, 2H), 3.07 (d, 1H, J=12.3 Hz), 3.35 (dd, 2H, J=4.2 Hz, J=11.7 Hz), 3.76 (s, 3H), 4.42-4.51 (m, 2H), 5.59 (bs, 1H), 9.3 (bs, 1H), 10.3 (bs, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08648074B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-773e00bff8a44a90980ea696f862de4b |
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| 出典メモ | uspto-grants-2014_02 |
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