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HRID 657982作成日:2026年10月25日

Methyl iodide → 1-Bromo-5-(1,1-dimethoxyethyl)-2-methoxy-3-trifluoromethylbenzene

https://huagongshe.com/reaction/657982

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Trimethyl orthoformateHCID 9005—
反応物Potassium CarbonateHCID 11430—
反応物3'-Bromo-4'-hydroxy-5'-(trifluoromethyl)acetophenoneHCID 58085700—
触媒D-Camphorsulfonic AcidHCID 65617—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
溶媒Heptane waterHCID 57468513—
生成物1-Bromo-5-(1,1-dimethoxyethyl)-2-methoxy-3-trifluoromethylbenzeneHCID 58085697—

反応手順

1-(3-Bromo-4-hydroxy-5-trifluoromethylphenyl)ethanone (O4.004; 6.8 g) was dissolved in methanol (50 ml) and admixed successively with DL-10-camphorsulfonic acid (111 mg) and trimethyl orthoformate (8 ml). After stirring at RT for 2 h, DMF (75 ml), potassium carbonate (4.98 g) and then slowly, while cooling with ice, iodomethane (3 ml) were added. After stirring at RT for 4 h, the reaction mixture was left to stand overnight and then admixed with n-heptane/water, and the organic phase was removed. The aqueous phase was extracted by shaking once more with n-heptane, and the combined organic phases were then dried over magnesium sulfate, filtered and concentrated. 7 g of the title compound were obtained in sufficient purity.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08076336B2
出典データセットuspto-grants-2011_12
ORD IDord-5992c9e592904eba8876e241466c6e2e
出典メモuspto-grants-2011_12