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HRID 501303作成日:2026年10月26日

Methyl iodide → 4-Bromo-2-(methoxymethyl)thiophene

https://huagongshe.com/reaction/501303

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Sodium hydrideHCID 24758—
反応物(4-Bromo-2-thienyl)methanolHCID 2795484—
溶媒TetrahydrofuranHCID 8028—
生成物4-Bromo-2-(methoxymethyl)thiopheneHCID 15018312—

反応手順

Add sodium hydride (737 mg, 29.23 mmol, 1.10 equivalents, 95%) to a solution containing methyl iodide (1.65 mL, 26.57 mmol, 1.00 equivalents) and (4-bromo-thiophen-2-yl)-methanol (5.13 g, 26.57 mmol, 1.00 equivalents) in tetrahydrofuran (dry, 25 mL). Stir the resulting mixture at room temperature overnight and evaporate. Partition the residue between water (100 mL) and dichloromethane (100 mL). Extract the aqueous layer with dichloromethane (100 mL), combine the organic layers, dry over magnesium sulfate, filter and evaporate to yield the desired product as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772252B2
出典データセットuspto-grants-2010_08
ORD IDord-18807178b5ad41e58744cd1064982c73
出典メモuspto-grants-2010_08