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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1732400생성일: 2026년 10월 27일

Triethylamine → 1-(4-Biphenylyloxy)-3,3-dimethyl-2-methoxymethylcarbamoyloxy-1-(1,2,4-triazol-1-yl)-butane

https://huagongshe.com/reaction/1732400

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methoxymethyl isocyanateHCID 62609—
반응물BitertanolHCID 91656—
반응물Di-n-butyldilauryltinHCID 9809426—
용매TetrahydrofuranHCID 8028—
생성물1-(4-Biphenylyloxy)-3,3-dimethyl-2-methoxymethylcarbamoyloxy-1-(1,2,4-triazol-1-yl)-butaneHCID 2030606982.9%

반응 단계

505 g (1.5 moles) of 1-(4-biphenylyloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol (A form) and 140 g (1.6 moles) of methoxymethyl isocyanate were heated under reflux in 2.5 liters of tetrahydrofuran in the presence of 40 ml of triethylamine and 1 ml of dibutyl-tin dilaurate for 48 hours. Thereafter, the solvent was stripped off in vacuo and 3 liters of petroleum ether were added to the residue. The crystalline precipitate formed was extracted by stirring with 1.5 liters of diisopropyl ether. 528 g (82.5% of theory) of 1-(4-biphenylyloxy)-3,3-dimethyl-2-methoxymethylcarbamoyloxy-1-(1,2,4-triazol-1-yl)-butane (A form) of melting point 95°-98° C. were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04237142
출처 데이터셋uspto-grants-1980_12
ORD IDord-241dca38976241c782d44dc4f4610135
출처 메모uspto-grants-1980_12