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Acetic Acid → ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Ethyl 4-(aminomethyl)benzoate | HCID 436161 | — |
| 反応物 | 2-(Benzyloxy)-5-bromobenzaldehyde | HCID 733087 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate | HCID 22675503 | — |
反応手順
2-Benzyloxy-5-bromobenzaldehyde and ethyl 4-aminomethylbenzoate were heated together at 100° C. for 1 hour. The mixture was cooled, dissolved in ethanol (100 ml) and sodium borohydride (1.3 g) was added. The mixture was stirred for 18 hours at ambient temperature, acidified with acetic acid and water (200 ml) was added. The mixture was extracted with diethyl ether (4×100 ml), the extracts washed with saturated aqueous NaHCO3, dried (MgSO4), filtered and evaporated to give ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate which was purified by chromatography on silica gel eluting with CH2Cl2 then 5% ethyl acetate/CH2Cl2 (yield 11.4 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05834468 |
| 出典データセット | uspto-grants-1998_11 |
| ORD ID | ord-ac2592b1d7e9403f99739f686d9d8a9c |
| 出典メモ | uspto-grants-1998_11 |