関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzene, 1-(chloromethyl)-2-fluoro- | HCID 9580 | — |
| 反応物 | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| 反応物 | 3-Amino-1-phenylpropan-1-ol | HCID 121548 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-(2-Fluorophenylmethyl)-3-hydroxy-3-phenylpropylamine | HCID 12951841 | 52.5% |
反応手順
A mixture of 3-hydroxy-3-phenylpropylamine (7.0 g, 46 mM) and 2,2,6,6-tetramethylpiperidine (7.9 ml, 46 mM) in acetonitrile (100 ml) was treated with a solution of o-fluorobenzyl chloride (6.75 g, 46 mM) in acetonitrile (10 ml). After 24 hours the resulting precipitate was removed by filtration and washed with acetonitrile (2×10 ml). The combined filtrate and washings were evaporated under reduced pressure and the residue partitioned between 2N hydrochloric acid (50 ml) and ether (100 ml). The aqueous layer was basified and extracted with ether, the ether extracts dried and evaporated. Chromatography on Grade 3 silica using 2% methanol in chloroform as eluant followed by distillation gave the title compound (6.3 g) b.p. 156°-160° C. (0.2 mbar).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04626522 |
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| 出典データセット | uspto-grants-1986_12 |
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| ORD ID | ord-868acbd05e6a4849a9c7572a5f4568ed |
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| 出典メモ | uspto-grants-1986_12 |
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