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HRID 19405作成日:2026年10月25日
Ethyl 2-(diphenylmethyleneamino)acetate → (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester
https://huagongshe.com/reaction/19405
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl 2-(diphenylmethyleneamino)acetate | HCID 319508 | — |
| 反応物 | (S)-(+)-1-Iodo-2-methylbutane | HCID 5702528 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester | HCID 86635244 | 74% |
反応手順
A solution of (benzhydrylidene-amino)-acetic acid ethyl ester (5.48 g, 20.5 mmol) in tetrahydrofuran (40 mL) was treated with potassium t-butoxide (2.83 g, 25.26 mmol) and stirred at 0° C. for 35 min. At this time a solution of (S)-1-iodo-2-methyl-butane (5.00 g, 25.25 mmol) in tetrahydrofuran (20 mL) was added via syringe and the resulting solution stirred at 0° C. for 10 min and then room temperature overnight. The reaction mixture was concentrated in vacuo and the residue partitioned between diethyl ether and dilute aqueous hydrochloric acid. The layers were separated, and the organic layer was washed with brine and concentrated in vacuo. The residue was purified by ISCO flash chromatography (RediSep silica 120 g, 0% to 10% ethyl acetate/hexanes) which afforded (S)-2-(benzhydrylidene-amino)-4-methyl-hexanoic acid ethyl ester (5.09 g, 74%) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07741327B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-e2b1e4a3f0e64d58bf4a398c4d0d1a9d |
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| 出典メモ | uspto-grants-2010_06 |
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