関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Guanidine Hydrochloride | HCID 5742 | — |
| 反応物 | Ethyl 3-cyclopentyl-3-oxopropanoate | HCID 11159709 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | HCID 135493693 | HCID 135493693 | 87.6% |
反応手順
To a solution of 3-cyclopentyl-3-oxo-propionic acid ethyl ester (5.0 g, 27.4 mmol) and guanidine hydrochloride (3.1 g, 33.0 mmol) in MeOH (50 mL) at 23° C. was added potassium tert-butoxide, portionwise (16.7 g. 149 mmol) over 15 min with vigorous stirring and the reaction warmed to 60° C. The reaction was cooled to room temperature (rt) and stirred overnight and the precipitated salt was removed by filtration. The solution was concentrated to approximately 10 mL then diluted with 10 mL of water and adjusted to pH=5 by the addition of 6.0 N HCl (6.1 mL). The resulting precipitate was filtered and dried via suction then vacuum to yield a white solid (4.3 g, 87%) that was used without further purification. 1H NMR (MeOD): 10.71-10.54 (m, 1H), 6.58-6.32 (m, 2H), 5.44-5.37 (m, 1H), 2.66 (p, J=8.1, 1H), 1.91-1.73 (m, 2H), 1.72-1.48 (m, 6H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08415366B2 |
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| 出典データセット | uspto-grants-2013_04 |
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| ORD ID | ord-26095282c1204c0c9e980ef18b1904e7 |
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| 出典メモ | uspto-grants-2013_04 |
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