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

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.

1. customwas again lowered to -50° C
2. stirringThe mixture was stirred for 1 hour
3. extractionextracted with ethyl acetate
4. washwashed with an aqueous saturated solution of sodium chloride
5. dry with materialdried over anhydrous magnesium sulfate
6. customAfter removing the solvent under reduced pressure
7. customthe residue was purified

ORD record

ord-cfdccdfada6946fe9f6ecb05d73fadd9

Source dataset

uspto-grants-1992_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05082856