関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Phenylglyoxal | HCID 14090 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 7-Methoxy-1,2,3,4-tetrahydronaphthalen-2-amine hydrochloride | HCID 14750915 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-[(7-Methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochloride | HCID 20160885 | 20% |
反応手順
An amount of 3.53 g of phenylglyoxal is reacted under stirring at room temperature for 3 hours with 5 g of 2-amino-7-methoxy-1,2,3,4-tetrahydronaphthalene hydrochloride in 100 ml of methanol in the presence of 0.9 g of sodium borohydride. After cooling to 4° C., 4,3 g of sodium borohydride are added and the reacting mixture is left under stirring at room temperature for a night. After addition of 20 ml of water, the solution is stirred at room temperature for 15 minutes, then it is evaporated to dryness. The residue is dissolved in 300 ml of ethyl acetate and 60 ml of water; after filtration, the organic phase is separated, dried over magnesium sulfate, filtered and evaporated to dryness. The oil thus obtained is purified by flash-chromatography by using a mixture ethyl acetate/methanol 8/2 as eluant to obtain the 2-[(7-methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochloride. Yield: 20% of the theoretical value.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04707497 |
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| 出典データセット | uspto-grants-1987_11 |
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| ORD ID | ord-a395cc8371f745c7a98988b156bd69c4 |
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| 出典メモ | uspto-grants-1987_11 |
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