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HRID 339929作成日:2026年10月26日

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

https://huagongshe.com/reaction/339929

反応式

関与物質

役割名称HCID仕込み量
反応物4-tert-Butylbenzyl alcoholHCID 13416—
反応物Sodium hydrideHCID 24758—
反応物4-Chloro-5-methoxypyrimidineHCID 11008039—
溶媒DimethylacetamideHCID 31374—
生成物4-(4-t-Butylbenzyloxy)-5-methoxypyrimidineHCID 7685323577%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895574B2
出典データセットuspto-grants-2014_11
ORD IDord-93733c3d90984d0eb0ecac29f21d3b54
出典メモuspto-grants-2014_11