戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 356173作成日:2026年10月25日

Chloroform → 9-Phenyl-4-(phthalimidoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one

https://huagongshe.com/reaction/356173

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物Potassium CarbonateHCID 11430—
反応物4-(phthalimidoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-oneHCID 18940541—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒BromobenzeneHCID 7961—
生成物9-Phenyl-4-(phthalimidoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-oneHCID 18940616126%

反応手順

To a suspension of 4-(phthalimidoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one (584 mg, 1.5 mmol) and potassium carbonate (228 mg, 1.6 mmol) in bromobenzene (3 mL) was added copper (I) iodide (57 mg, 0.3 mmol), and the mixture was heated for 90 minutes under reflux. To the reaction mixture was added chloroform, which was subjected to filtration, and the filtrate was concentrated under reduced pressure. The concentrate was recrystallized from chloroform-ethanol-hexane to give 440 mg (yield 63%) of a mixture of cis-compound and trans-compound (3:2), m.p. 272°-273° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05834463
出典データセットuspto-grants-1998_11
ORD IDord-497a574e32204599bf338740bc3a80f7
出典メモuspto-grants-1998_11