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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1973941생성일: 2026년 10월 26일

Tetrafluoroborate → 1-(1-Benzyl-2-pyrrolidylidene)-3-(2,6-dimethylphenyl)urea

https://huagongshe.com/reaction/1973941

반응식

참여 물질

역할이름HCID투입량
반응물TetrafluoroborateHCID 26255—
반응물2,6-Xylyl isocyanateHCID 98787—
반응물1-Benzyl-2-iminopyrrolidineHCID 12449023—
생성물1-(1-Benzyl-2-pyrrolidylidene)-3-(2,6-dimethylphenyl)ureaHCID 54373462—

반응 단계

The fluoroborate salt of 1-benzyl-2-iminopyrrolidine (6.55 g.; 0.025 mole) is converted to free base (4.36 g.; 0.025 mole) in the usual manner. After drying over K2CO3, the benzene solution is filtered through diatomaceous earth and 3.68 g. (0.025 mole) of 2,6-dimethylphenylisocyanate is added. The reaction mixture is stirred at room temperature for 1 hour and then evaporated to dryness in vacuo to give an oily residue of 1-(1-benzyl-2-pyrrolidylidene)-3-(2,6-dimethylphenyl)urea which is dissolved in ether and converted to the hydrochloride salt. Recrystallizations from methanol yields the product, 1-(1-benzyl-2-pyrrolidylidene)-3-(2,6-dimethylphenyl)urea HCl, m.p. = 185°-195° C. (dec.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03998958
출처 데이터셋uspto-grants-1976_12
ORD IDord-7e2b7db0271643a595da5d3cb8399d4a
출처 메모uspto-grants-1976_12