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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 492287생성일: 2026년 10월 24일

Triethylamine → HCID 68851040, 화합물

https://huagongshe.com/ko/reaction/492287

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물2,4,6-Trifluorobenzoic acidHCID 520373—
반응물HCID 68851238HCID 68851238—
용매BenzeneHCID 241—
생성물HCID 68851040HCID 6885104074%

반응 단계

2,4,6-Trifluorobenzoic acid (148.8 mg), diphenylphosphoryl azide (223.3 mg) and triethylamine (105.1 mg) were added to benzene (8 mL) and the mixture was heated under reflux. Fifty minutes later, a solution of N-heptyl-N-[[2′-[N-(triphenylmethyl)tetrazol-5-yl]-1,1′-biphenyl-4-yl]methyl]amine (393.7 mg) in benzene (3 mL) was added to the reaction mixture, and under reflux, heating was continued. Upon elapsed time of 45 minutes after the addition of the solution, the reaction mixture was concentrated under reduced pressure. Ethyl acetate (40 mL) was added to the residue, and the resulting mixture was washed successively with 5% hydrochloric acid, water, a saturated sodium bicarbonate solution and brine (40 mL, each). The organic layer was dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was subjected to chromatography on a silica gel column (hexane/ethyl acetate) to afford N′-heptyl-N-(2,4,6-trifluorophenyl)-N′-[[2′-[N-(triphenylmethyl)tetrazol-5-yl]-1,1′-biphenyl-4-yl]methyl]urea as a colorless amorphous mass (369.1 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07531576B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-b98e816bba8844feb006a99d8dff52de
출처 메모uspto-grants-2009_05