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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339929생성일: 2026년 10월 23일

4-tert-Butylbenzyl alcohol → 4-(4-t-Butylbenzyloxy)-5-methoxypyrimidine

https://huagongshe.com/ko/reaction/339929

반응식

참여 물질

역할이름HCID투입량
반응물4-tert-Butylbenzyl alcoholHCID 13416—
반응물Sodium hydrideHCID 24758—
반응물4-Chloro-5-methoxypyrimidineHCID 11008039—
용매DimethylacetamideHCID 31374—
생성물4-(4-t-Butylbenzyloxy)-5-methoxypyrimidineHCID 7685323577%

반응 단계

To a solution of 4-chloro-5-methoxypyrimidine (1.5 g, 10.3 mmol) described in Journal of the Chemical Society (1960), 4590, and 4-t-butylbenzylalcohol (2.55 g, 15.6 mmol) in dimethylacetamide (10 mL) was added sodium hydride (0.625 g, 15.6 mmol) at 0° C., and the mixture was stirred at room temperature for 3 hrs. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 4-(4-t-butylbenzyloxy)-5-methoxypyrimidine (2.16 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895574B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-93733c3d90984d0eb0ecac29f21d3b54
출처 메모uspto-grants-2014_11