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HRID 30295作成日:2026年10月25日

Chloro(diphenyl)silane → 2-Benzyl-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[alpha]pentalene

https://huagongshe.com/reaction/30295

反応式

関与物質

役割名称HCID仕込み量
反応物Chloro(diphenyl)silaneHCID 74206—
反応物indium(III)chlorideHCID 159675—
反応物2-Benzyl-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[alpha]pentalen-7-olHCID 131727050—
溶媒1,1-DichloroethaneHCID 6365—
生成物2-Benzyl-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[alpha]pentaleneHCID 13172704957%

反応条件

温度60 °C

反応手順

Indiumtrichloride (973 mg, 4.40 mmol) and chlorodiphenylsilane (2888 mg, 13.20 mmol) were added to a solution of the product from step f) (1192 mg, 4.40 mmol) in 20 mL of dichloroethane. The reaction mixture was heated at 60° C. overnight and then was cooled to room temperature and quenched with saturated NaHCO3 (50 ml). The reaction mixture was extracted with ethylacetate (2×50 mL). The combined organic extracts were washed with brine (50 ml), dried with MgSO4 and solvent evaporated in vacuo to afford the subtitle compound (638 mg, yield: 57%) that was used without further purification. MS calculated C16H17NS+H: 256, observed: 256.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423056B2
出典データセットuspto-grants-2008_09
ORD IDord-e1aa197d0bd24dc7b74e830b3a5cd79a
出典メモuspto-grants-2008_09