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HRID 347870作成日:2026年10月27日

Iodine → 2,6-Dimethoxy-4-methoxymethylphenylboric acid

https://huagongshe.com/reaction/347870

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Trimethyl borateHCID 8470—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
反応物2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzeneHCID 23080940—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物2,6-Dimethoxy-4-methoxymethylphenylboric acidHCID 2308094589%

反応条件

温度70 °C

反応手順

To a suspension of magnesium turnings (97.5 mg, 4.01 mmol) in tetrahydrofuran (0.5 mL) containing a small amount of added iodine, was added approximately a tenth part of a solution of 2-bromo-1,3-dimethoxy-5-(methoxymethyl)benzene (1.0 g, 3.82 mmol) in tetrahydrofuran (1 mL) under a nitrogen atmosphere, and the mixture was heated in an oil bath at 70° C. The heating was terminated upon gentle reflux of the reaction mixture and fading of the iodine color. To continue the reflux, the remaining solution of 2-bromo-1,3-dimethoxy-5-(methoxymethyl)benzene in tetrahydrofuran was added dropwise to the reaction mixture. Upon completion of the dropwise addition, the reaction mixture was further heated to reflux for 1 hour and then cooled to room temperature. The reaction mixture was then added dropwise to an ice-cooled solution of trimethyl borate (0.57 mL, 4.97 mmol) in tetrahydrofuran (0.5 mL). Upon completion of the dropwise addition and stirring for 40 minutes while cooling with ice, the mixture was stirred overnight at room temperature. An aqueous ammonium chloride solution and methanol were then added to the reaction mixture. Quantitation by liquid chromatography confirmed that the title compound had been obtained at an 89% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07176216B2
出典データセットuspto-grants-2007_02
ORD IDord-b54b18ef27434a6ea3cb26a03f88f82d
出典メモuspto-grants-2007_02