Green synthesis of 6-cyano-2,2-dimethyl-2-H-1-benzopyran and itssubsequent enantioselective epoxidation

GUSTAVO ROMANELLI; ÁNGEL SATHICQ; PATRICIA VÁZQUEZ; AÍDA VILLA; EDWIN ALARCÓN; EDWING GRAJALES; JAIRO CUBILLOS

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL

ELSEVIER SCIENCE BV

Lugar: Amsterdam; Año: 2015 p. 11 - 16

1381-1169

The clean synthesis of 6-cyano-2,2-dimethyl-2-H-1-benzopyran epoxide starting from 3-methyl-2-butenal is reported using recyclable catalysts. H4PMo11VO40(PMo11V) and (PyH)3HPMo11VO40(Py3?PMo11V) Keggin-type heteropolyacids were used to synthesize 6-cyano-2,2-dimethyl-2-H-1-benzopyran in two steps with 35% yield. This is an alternative procedure to the traditionalmethodology with pyridine or picoline as catalyst, where 6-cyano-2,2-dimethyl-2-H-1-benzopyran isobtained by condensation of 4-cyanophenol with 1,1-diethoxy-3-methyl-2-butene. The 6-cyano-2,2-dimethyl-2-H-1-benzopyran epoxide was obtained using Jacobsen-type catalysts, and in situ generateddimethyldioxirane (DMD) as oxidizing agent, that in comparison to m-CPBA/4-NMO and NaOCl/4-PPNOdid not degrade the catalyst. In presence of 4-phenylpyridine N-oxide (4-PPNO) at 4◦C, enantioselectiv-ities of 87% for 3S,4S-epoxide and 68% for 3R,4R-epoxide were obtained with the S,S- and R,R-Jacobsencatalysts, respectively. Overall yield was approximately 17% for 3S,4S-epoxide.