Ge. Henry et H. Jacobs, A short synthesis of 5-methoxy-2,2-dimethyl-2H-1-benzopyran-6-propanoic acid methyl ester, TETRAHEDRON, 57(25), 2001, pp. 5335-5338
5-Methoxy-2,2-dimethyl-2H-1-benzopyran-6-propanoic acid methyl ester was pr
epared in five steps and approximately 20% overall yield from 2,4-dihydroxy
benzaldehyde. The two key reactions are the chromenylation between the unch
elated hydroxyl group and C-3 of the resbenzaldehyde and the demethoxycarbo
nylation-alkylation of dimethyl malonate with a quaternary ammonium iodide.
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