関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pentane | HCID 8003 | — |
| 反応物 | Tert-butyl p-tolylcarbamate | HCID 4935486 | — |
| 反応物 | N-Methoxy-N-methylcyclopropanecarboxamide | HCID 15643267 | — |
| 反応物 | HCID 178418306 | HCID 178418306 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | (2-Amino-5-methyl-phenyl)-cyclopropyl-methanone | HCID 15346381 | 95.1% |
反応手順
To a stirred solution of p-tolyl-carbamic acid tert-butyl ester (1.0 g, 4.8 mmol) in Et2O (10 mL) under a nitrogen atmosphere was added dropwise a 1.7 M solution of t-BuLi in pentan (6.5 mL, 11.1 mmol) over a 10-min period at −20° C. The mixture was stirred at −10° C. for 2.5 h and then cyclopropanecarboxylic acid methoxy-methyl-amide (0.92 g, 6.3 mmol) was added over 5 min. The mixture was allowed to warm to room temperature and stirred for further 1 h before it was quenched with aqueous NH4Cl. The organic phase was isolated and the aqueous phase was extracted with CH2Cl2, and the combined organic phases were dried and concentrated in vacuo. The crude material was dissolved CH2Cl2 (15 mL) and TFA (15 mL) and stirred at room temperature for 3 h. The reaction mixture was evaporated in vacuo, and added aqueous NaHCO3 to pH 7 and extracted with CH2Cl2. The combined organic phases were dried and concentrated in vacuo to give 0.80 g crude (2-amino-5-methyl-phenyl)-cyclopropyl-methanone as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08063081B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-071a1dbd861f4554a344dd921e79eaca |
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| 出典メモ | uspto-grants-2011_11 |
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