Hydrochloric Acid → 2-(4-Chlorophenyl)cyclopropan-1-amine hydrochloride
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:10][CH:9]2[NH:11]C(=O)OC(C)(C)C)=[CH:4][CH:3]=1.Cl.O1CCOCC1>ClCCl>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH2:10][CH:9]2[NH2:11])=[CH:6][CH:7]=1参加物
5
実験手順
tert-Butyl 2-(4-chlorophenyl)cyclopropylcarbamate (51.9 mg, 0.1938 mmol) was dissolved in Dichloromethane (1 ml) and 4M HCl solution in dioxane (0.4846 ml, 1.938 mmol) was added. The mixture was stirred for 3 hours at ambient temperature, during which time a white solid precipitated out of solution. The crude mixture was concentrated and chased with EtOAc (2×10 ml). The residual fine solid was dried under high vacuum to provide 39.2 mg of the title compound as a solid (99%).
後処理
- customprecipitated out of solution
- concentrationThe crude mixture was concentrated
- customThe residual fine solid was dried under high vacuum
出典と根拠
- ORDレコード
- ord-620126016fe54cf19f21bb3a5dc9d4ed
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09096567B2
反応ノート
読み込み中…