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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15142생성일: 2026년 10월 25일

4-Methoxybenzyl alcohol → 4-Methoxybenzyl bromide

https://huagongshe.com/reaction/15142

반응식

참여 물질

역할이름HCID투입량
반응물4-Methoxybenzyl alcoholHCID 7738—
반응물Phosphorus tribromideHCID 24614—
용매Diethyl EtherHCID 3283—
생성물4-Methoxybenzyl bromideHCID 165021—

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732460B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0f401c1908dd4cb7a39a733db0bd4a41
출처 메모uspto-grants-2010_06