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HRID 29798作成日:2026年10月24日

Water → Tert-butyl [1,1-dimethyl-3-(5-methyl-3-p-tolyl-[1,2,4]triazol-1-yl)-propyl]-carbamate

https://huagongshe.com/ja/reaction/29798

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物5-Methyl-3-(4-methylphenyl)-1H-1,2,4-triazoleHCID 43166776—
反応物tert-butyl N-(4-chloro-2-methylbutan-2-yl)carbamateHCID 57429079—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒Ethyl AcetateHCID 8857—
溶媒2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
生成物Tert-butyl [1,1-dimethyl-3-(5-methyl-3-p-tolyl-[1,2,4]triazol-1-yl)-propyl]-carbamateHCID 69538809—

反応手順

1.35 g (34 mmol, 60%) sodium hydride are added at 0° C. to a solution of 4.87 g (28 mmol) 5-methyl-3-p-tolyl-[1,2,4]triazole in 40 mL of DMPU. The reaction mixture is heated to ambient temperature and then stirred for one hour. 9.35 g (42 mmol) tert-butyl (3-chloro-1,1-dimethyl-propyl)-carbamate and 1.87 g (5 mmol) tetrabutylammonium iodide are added and the mixture is stirred overnight at ambient temperature and then for 2 hours at 80° C. The mixture is combined with water and ethyl acetate, the aqueous phase is separated off and extracted with ethyl acetate. The combined organic phases are washed with water and sodium chloride solution, dried with sodium sulphate and evaporated down. The residue is purified by column chromatography (silica gel; petroleum ether/ethyl acetate=1:1). Oil. Yield: 2.97 g (30%); mass spectroscopy [M+H]+=359.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423036B2
出典データセットuspto-grants-2008_09
ORD IDord-9abc96cf68074ffdb19d2362b2f5e482
出典メモuspto-grants-2008_09