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HRID 129344생성일: 2026년 10월 25일

Tetrahydrofuran → Methyl 4-(1-cis tridecenyl)pyrrole-2-carboxylate

https://huagongshe.com/reaction/129344

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Dodecyltriphenylphosphonium bromideHCID 84955—
반응물methyl 4-formyl-1H-pyrrole-2-carboxylateHCID 640310—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매HexaneHCID 8058—
생성물Methyl 4-(1-cis tridecenyl)pyrrole-2-carboxylateHCID 1502333465%

반응 단계

A ca. 15% solution (18.5 ml) of n-butyllithium in hexane was added dropwise at -50° C. to a tetrahydrofuran suspension (95 ml) of 16.0 g (31.4 mmol) of dodecyltriphenylphosphonium bromide described in Chemistry and Industry (London) p. 1086, 1958. The temperature was raised to room temperature and the mixture was stirred for 30 minutes. The temperature was again lowered to -50° C. To the mixture was added dropwise a tetrahydrofuran solution (50 ml) of 2.4 g (15.7 mmol) of methyl 4-formylpyrrole-2-carboxylate described in Bulletin de la Societe Chimique de France, p. 283, 1972. The mixture was stirred for 1 hour, diluted with water, extracted with ethyl acetate, washed with an aqueous saturated solution of sodium chloride and dried over anhydrous magnesium sulfate. After removing the solvent under reduced pressure, the residue was purified by subjecting it to column chromatography over silica gel (eluent: ethyl acetate/hexane=1/7) to obtain 3.11 g (65% yield) of methyl 4-(1-cis tridecenyl)pyrrole-2-carboxylate, m.p. 51°-52° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE035096
출처 데이터셋uspto-grants-1995_11
ORD IDord-b3178c436b744eec97f807fde774d867
출처 메모uspto-grants-1995_11