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HRID 615346作成日:2026年10月26日
Hydrochloric Acid → (4R,4'R)-3,3'-(Octanedioyl)bis[2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid]
https://huagongshe.com/reaction/615346
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Octanedioyl dichloride | HCID 534653 | — |
| 反応物 | (4R)-2-(2-hydroxyphenyl)-1,3-thiazolidine-4-carboxylic acid | HCID 2825745 | — |
| 溶媒 | Potassium Carbonate | HCID 11430 | — |
| 生成物 | (4R,4'R)-3,3'-(Octanedioyl)bis[2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid] | HCID 12837209 | 86% |
反応手順
To a stirred solution of (4R)-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid (6.8 g) in 1M potassium carbonate (45 ml), octanedioyl dichloride (3.2 g) was added dropwise under ice-cooling. After the addition, the reaction mixture was stirred for 1 hour at the same temperature and for additional 1 hour at room temperature. The solution was acidified with dilute hydrochloric acid, extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residual oil was purified by silica gel column chromatography to give 7.6 g (86%) of the titled compound: mp 93°-97° C. (dec.); [α]D27 +123.6° (c=0.5, methanol). IR (nujol, cm-1): 1720 (COOH), 1620 (CON), 1600 (aromatic), 1230, 1090, 855, 765. NMR (CD3OD) δ: 0.7-1.7 (8H, m, --CH2 --CH2)4CH2 --), 1.8-2.4 (4H, m, --CH2 --CH2)4CH2), 3.25 (4H, d, J=7.5 Hz, C5 --H), 4.81 (2H, t, J=7.5 Hz, C4 --H), 6.35 (2H, s, C2 --H), 6.7-8.0 (8H, m, arom. H). TLC: Rf value* 0.34.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04499102 |
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| 出典データセット | uspto-grants-1985_02 |
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| ORD ID | ord-a28c83ca718d4de8bf45702e3d24af4c |
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| 出典メモ | uspto-grants-1985_02 |
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