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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 426189생성일: 2026년 10월 26일

4-Methoxybenzyl alcohol → 4-Chloro-5-isopropyl-2,6-bis-(4-methoxy-benzyloxy)-pyrimidine

https://huagongshe.com/reaction/426189

반응식

참여 물질

역할이름HCID투입량
반응물4-Methoxybenzyl alcoholHCID 7738—
반응물Sodium hydrideHCID 24758—
반응물2,4,6-Trichloro-5-isopropylpyrimidineHCID 249009—
용매DimethylformamideHCID 6228—
생성물4-Chloro-5-isopropyl-2,6-bis-(4-methoxy-benzyloxy)-pyrimidineHCID 5918471379%

반응 단계

To a stirred solution of p-methoxybenzyl alcohol (110 ml) in anhydrous DMF (50 ml) in a water bath under nitrogen atmosphere, was portionwise added 60% sodium hydride (4 g, 100 mmol). After complete reaction of sodium hydride, the mixture was cooled in an ice-water bath and 5-isopropyl-2,4,6-trichloropyrimidine (11.275 g, 50 mmol) was added. After 1 hr., the mixture was stirred for overnight at room temperature. The excess p-methoxybenzyl alcohol and DMF were distilled off in high vacuo and the residue was partitioned between ether and water. The ether layer was taken, washed with water, dried with anhydrous magnesium sulfate, filtered, and evaporated in vacuo to give a crude product as a colorless syrup. The crude product was purified by silica gel column chromatography (eluent, ether:hexanes (1:9)) to afford 17 g (79%) of a white solid. m.p. 69-70° C.; 1H NMR (200 MHz, CDCl3) δ 1.23 (6H, d, J=7.0 Hz), 3.42 (1H, m), 3.81 (3H, s), 3.82 (3H, s), 5.31 (2H, s), 5.35 (2H, s), 6.87-6.92 (4H, m), 7.30-7.43 (4H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08106064B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-8e72ac00f0a2476d9bd75c9ef1ea568e
출처 메모uspto-grants-2012_01