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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1973948생성일: 2026년 10월 26일

Tetrafluoroboric acid → 1-(2,6-Dimethylphenyl)-3-(1,5-dimethyl-2-pyrrolidylidene)urea

https://huagongshe.com/reaction/1973948

반응식

참여 물질

역할이름HCID투입량
반응물Tetrafluoroboric acidHCID 28118—
반응물2,6-Xylyl isocyanateHCID 98787—
반응물1,5-Dimethyl-2-iminopyrrolidineHCID 12449024—
용매BenzeneHCID 241—
생성물1-(2,6-Dimethylphenyl)-3-(1,5-dimethyl-2-pyrrolidylidene)ureaHCID 54555224—

반응 단계

The HBF4 salt of 1,5-dimethyl-2-iminopyrrolidine (6.75 g.; 0.0337 mole) is converted to free base in benzene in the usual manner. Then 4.96 g. (0.0337 mole) of 2,6-dimethylphenylisocyanate, dissolved in anhydrous benzene, is added. The reaction mixture is stirred for 2 hours and then the solvent is evaporated in vacuo leaving an oily residue which eventually crystallizes. Recrystallization from ethyl acetate gives the product, 1-(2,6-dimethylphenyl)-3-(1,5-dimethyl-2-pyrrolidylidene)urea, m.p. 120°-122° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03998958
출처 데이터셋uspto-grants-1976_12
ORD IDord-9e1a82942fec42c99e8ba3f2b044f9a0
출처 메모uspto-grants-1976_12