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HRID 15142作成日:2026年10月26日

4-Methoxybenzyl alcohol → 4-Methoxybenzyl bromide

https://huagongshe.com/reaction/15142

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methoxybenzyl alcoholHCID 7738—
反応物Phosphorus tribromideHCID 24614—
溶媒Diethyl EtherHCID 3283—
生成物4-Methoxybenzyl bromideHCID 165021—

反応手順

A solution of 4-methoxybenzyl alcohol (6.2 ml, 50 mmol) in dry ether (120 ml) was treated dropwise with phosphorus tribromide (2.07 ml, 22 mmol), refluxed for 1 hour, cooled, washed twice with water, dried and the solvent evaporated. The 4-methoxybenzyl bromide thus produced was added to a mixture of 4-bromo-1,2-dihydro-3,6-pyridazinedione (for a preparation, see B. Kasnar et al, Nucleosides & Nucleotides (1994), 13(1-3), 459-79 or Example 30(a)) (4 g, 21 mmol) and potassium carbonate (8.28 g, 60 mmol) in dry DMF (60 ml) and stirred overnight at room temperature. The mixture was diluted with ethyl acetate, washed 3 times with water, dried over magnesium sulfate and evaporated to low volume. Some solid was filtered off and washed with ethyl acetate. The filtrate was evaporated to dryness and the residue chromatographed on silica gel, eluting with 20% ethyl acetate/hexane and then 100% ethyl acetate. This gave the less polar of the 2 desired products (3.233 g), the more polar of the 2 desired products (1.626 g) and a mixture of these (1.351 g). Total yield 6.30 g, 70%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732460B2
出典データセットuspto-grants-2010_06
ORD IDord-0f401c1908dd4cb7a39a733db0bd4a41
出典メモuspto-grants-2010_06