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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29798생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/29798

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물5-Methyl-3-(4-methylphenyl)-1H-1,2,4-triazoleHCID 43166776—
반응물tert-butyl N-(4-chloro-2-methylbutan-2-yl)carbamateHCID 57429079—
촉매Tetrabutylammonium IodideHCID 67553—
용매Ethyl AcetateHCID 8857—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물Tert-butyl [1,1-dimethyl-3-(5-methyl-3-p-tolyl-[1,2,4]triazol-1-yl)-propyl]-carbamateHCID 69538809—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423036B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-9abc96cf68074ffdb19d2362b2f5e482
출처 메모uspto-grants-2008_09