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HRID 1013364作成日:2026年10月26日

Chloro(diphenyl)silane → 2-Benzyl-5,6-dibromo-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[alpha]pentalene

https://huagongshe.com/reaction/1013364

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Sodium BicarbonateHCID 516892—
反応物2-Benzyl-5,6-dibromo-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[alpha]pentalen-7-olHCID 131727029—
溶媒1,1-DichloroethaneHCID 6365—
溶媒Ethyl AcetateHCID 8857—
生成物2-Benzyl-5,6-dibromo-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[alpha]pentaleneHCID 131727030—

反応条件

温度60 °C

反応手順

The product from step f) (300 mg, 0.69 mmol) in dichloroethane (2.6 ml) was treated with InCl3 (153 mg, 0.69 mmol) and chlorodiphenylsilane (457 mg, 2.08 mmol). The contents were heated to 60° C. for 16 hours. The reaction mixture was cooled to 22° C., poured into sat. NaHCO3 and diluted with EtOAc (75 ml); producing a white emulsion. The emulsion was passed through celite and the organic layer was separated, washed with brine (25 ml) and dried (MgSO4). The crude product was dissolved in 7:3 hexanes:EtOAc and passed through a plug of silica gel to give the subtitle compound. MS calculated for C16H15Br2NS+H 414, observed 412, 414, 416.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07981919B2
出典データセットuspto-grants-2011_07
ORD IDord-d93270e23f514652841b6f02b2a5de08
出典メモuspto-grants-2011_07