Oxindolic fragment is an often part of many natural compounds having various useful biological properties such as antiviral, anti-cancer, antimicrobial etc. It is worth noting and different spirooxindoles, because the presence of spirocycle in its molecules, its scale and variety of substitutes in spirocycles lead us to a huge amount of substances with potential biologic activity. It is known, that spirocyclopropaneoxindoles possessing anti-HIV activity, that is why, the synthesis of such optically pure compounds is a very good challenge.formulaInitially, the selective extraction from turpentine succeeding by uneasy processes leads us to pure [1] dehydroabietic acid 1, but the next interaction with oxalylchloride in dry chloroform gave us chloride 2 in quantitative yield practically. The synthesis of cyclopropaneoxindole 4 resulted in four stages [2, 3] (see scheme), but the final conversion was realized by classical amidation reaction between chloride 2 and oxindole 4 in dry chloroform with equimolar amount of Et3N and led us to new functionalized spirocyclopropaneoxindole 3. The target compound was isolated by column chromatography and proved by NMR.