関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | (Benzyloxy)acetic acid | HCID 290301 | — |
| 反応物 | Methyl(4-aminophenoxy)acetate | HCID 6422115 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(2-Benzyloxyacetylamino)phenoxyacetic acid methyl ester | HCID 59253983 | 68.9% |
反応手順
To a mixture of (4-aminophenoxy)-acetic acid methyl ester 3 (20 g, 110.5 mmol) and benzyloxy acetic acid (20.4 g, 123 mmol) in anhydrous dichloromethane (200 ml) under nitrogen atmosphere was added dropwise a solution of 1,3-dicyclohexyl carbo-diimide (63.2 g, 306 mmol) in anhydrous dichloromethane (80 ml) then stirred at room temp. for 12 hours. The solids were filtered off, the dichloromethane was washed with 5% sodium bicarbonate solution (100 ml), water (100 ml) added, and the solids dried over sodium sulphate and distilled to get crude 49. Crude 49 was purified by column chromatography on silica gel using benzene as eluant to get pure 49 (25 g, 68.9%) as a white powder with an m.p. between 76-77.5° C. 1H NMR (CDCl3) δ 3.82 (s, 3H, ester), 4.10 (s, 2H, CH2), 4.62 (s, 2H, CH2), 4.66 (s, 2H, CH2), 6.88 (d, 2H, Ar), 7.38 (m, 5H, Ar), 7.46 (d, 2H, Ar), 8.24 (bs, 1H, NH)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846845B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-c57186fa43784b8e8a50548a6a12cdb3 |
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| 出典メモ | uspto-grants-2014_09 |
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