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HRID 639845作成日:2026年10月26日

Acetate → Dimethyl 2-(3,4-dichlorophenyl)-2-(2-{[(1,1-dimethylethyl)(diphenyl)silyl]oxy}ethyl)-1,1-cyclopropanedicarboxylate

https://huagongshe.com/reaction/639845

反応式

関与物質

役割名称HCID仕込み量
反応物AcetateHCID 175—
反応物2-Diazonio-1,3-dimethoxy-3-oxoprop-1-en-1-olateHCID 547673—
反応物{[3-(3,4-Dichlorophenyl)-3-buten-1-yl]oxy}(1,1-dimethylethyl)diphenylsilaneHCID 59255999—
溶媒DichloromethaneHCID 6344—
生成物Dimethyl 2-(3,4-dichlorophenyl)-2-(2-{[(1,1-dimethylethyl)(diphenyl)silyl]oxy}ethyl)-1,1-cyclopropanedicarboxylateHCID 5925600582.3%

反応条件

温度100 °C

反応手順

{[3-(3,4-Dichlorophenyl)-3-buten-1-yl]oxy}(1,1-dimethylethyl)diphenylsilane (P13, 2.25 g), dimethyl diazopropanedioate (1.2 g) (prepared in an analogous manner as reported in Synthetic Communications, 17(4), 1709-16, 1987) and rodhium (II) acetate dimer (0.060 g) were mixed together and heated at 100° C. for 40 min. After cooling, the residue was treated with DCM and the mixture was filtered. The filtrate was evaporated under reduced pressure and the crude product was purified by flash chromatography (Cy/EA from 1/0 to 95/5) to give the title compound (2.38 g) as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691893B2
出典データセットuspto-grants-2010_04
ORD IDord-ccfab170865e4aa2a012ddae800d2bfb
出典メモuspto-grants-2010_04