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HRID 42757作成日:2026年10月26日

Ethylene Glycol → 2-(3-Bromophenyl)-2-methyl-1,3-dioxolane

https://huagongshe.com/reaction/42757

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物NitrogenHCID 947—
反応物Trimethyl orthoformateHCID 9005—
反応物Sodium CarbonateHCID 10340—
反応物3'-BromoacetophenoneHCID 16502—
生成物2-(3-Bromophenyl)-2-methyl-1,3-dioxolaneHCID 10999218—

反応条件

温度95 °C

反応手順

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 1-(3-bromo-phenyl)-ethanone (1360 mg, 6.83 mmol) in ethylene glycol (8.00 mL, 143.46 mmol) was treated with trimethylorthoformate (1.50 mL, 13.68 mmol) followed by LiBF4 (131 mg, 1.37 mmol). The reaction mixture was heated at 95° C. for 15 h. Sat. aq. Na2CO3 was added and the mixture was extracted twice with ether and the combined organic extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1 hept-EA) gave the title compound as a pale yellow oil: TLC:rf (10:1 hept-EA)=0.34. LC-MS-conditions 02: tR=1.01 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536209B2
出典データセットuspto-grants-2013_09
ORD IDord-2395729cc9094f8db19164bab0b1ef65
出典メモuspto-grants-2013_09