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HRID 337552作成日:2026年10月25日

1,4-Bis(diphenylphosphino)butane → 1,1-Dimethylethyl cyclopropyl{[2,3-dichloro-5-(2-hydroxyethyl)phenyl]methyl}carbamate

https://huagongshe.com/reaction/337552

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Bis(diphenylphosphino)butaneHCID 82124—
反応物Sodium PerborateHCID 517072—
反応物4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
反応物1,1-Dimethylethyl cyclopropyl[(2,3-dichloro-5-ethenylphenyl)methyl]carbamateHCID 66895414—
溶媒TetrahydrofuranHCID 8028—
生成物1,1-Dimethylethyl cyclopropyl{[2,3-dichloro-5-(2-hydroxyethyl)phenyl]methyl}carbamateHCID 66897112—

反応手順

1,1-Dimethylethyl cyclopropyl[(2,3-dichloro-5-ethenylphenyl)methyl]carbamate (1 eq.) from the previous step, [Ir(COD)Cl]2 (0.025 eq.) and DPPB (0.05 eq.) were combined in THF (0.11 M). To this solution was then added 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.3 eq.) and the resulting red solution was stirred at RT for 12 h. Finally, sodium perborate (0.1 M aqueous solution, 1 eq.) was added and the now black biphasic solution was vigorously stirred at RT for another 12 h. The aqueous layer was separated and back-extracted with ether. The combined organic extracts were then washed further with 1 N aq. NaOH, water and brine. This was then dried over Na2SO4, filtered and the filtrate concentrated in vacuo to afford a pale yellow oil. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 9:1 (v/v) Hex:EtOAc→3:7 (v/v) EtOAc:Hex) afforded the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889714B2
出典データセットuspto-grants-2014_11
ORD IDord-b146069054414e8eb218ee37d816b6d7
出典メモuspto-grants-2014_11