戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 713073作成日:2026年10月24日

Cyclopropanecarbonyl chloride → Ethyl 4-(cyclopropanecarbonyl)benzoate

https://huagongshe.com/ja/reaction/713073

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclopropanecarbonyl chlorideHCID 77637—
反応物HCID 178469117HCID 178469117—
触媒HCID 178479802HCID 178479802—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 4-(cyclopropanecarbonyl)benzoateHCID 2472409278.4%

反応手順

(4-Ethoxycarbonylphenyl)-iodo-zinc (20 mL of 0.5 M in THF, 10.0 mmol) was added over 10 min to dichloro-bis(triphenylphosphoranyl)palladium (211 mg, 0.3 mmol) in THF (20 mL) under an atmosphere of nitrogen at 0° C. The reaction mixture was stirred for 15 minutes, cyclopropanecarbonyl chloride (941 mg, 817 μL, 9.0 mmol) was added dropwise at 0° C. and stirred for 2 hours. The reaction mixture was quenched with 1M HCl (20 mL), extracted with ethyl acetate (2×50 mL). The organic layer was washed sequentially with sat. aq. NaHCO3 (5 mL) and brine solution (50 mL), dried over MgSO4 and purified by silica gel column chromatography using 0-30% EtOAc/hexanes as eluent to give ethyl 4-(cyclopropanecarbonyl)benzoate (1.54 g, 71%) as a pale yellow oil. ESI-MS m/z calc. 218.0. found 219.3 (M+1)+; Retention time: 1.57 minutes (3 min run).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181273B2
出典データセットuspto-grants-2015_11
ORD IDord-68a84cabc4444674870de6c805b18ff4
出典メモuspto-grants-2015_11