In a recent attempt to add t-butyl hypochlorite to olefins such as styrene and l-hexene in nitromethane, we were surprised to find that the exclusive products of these rapid reactions are chloronitromethane (ClCHaNO =,I) and t-butyl alcohol in nearly quantitative yield. This reaction is outlined in
Reaction of methyl hypochlorite with certain olefins in the presence of boron trifluoride
โ Scribed by Victor L. Heasley; Dale F. Shellhamer; Robert K. Gipe; Harry C. Wiese; Melanie L. Oakes; Gene E. Heasley
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- French
- Weight
- 213 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Fluoro chlorides are maJor products in the reactlon of methyl hypochlonte with certain oleflns 1t-1 the presence of boron trifluoride We would like to report an unexpected reactlon of methyl hypochlorite (CH30C1,L) with certain oleflns in methylene chloride contalnlng a small amount of boron tnfluorlde, BF3 132 We observed that 1. reacted with methyl acrylate (z), methyl crotonate (L), and methyl isocrotonate (2) to produce fluoro chlorides by the addition of the elements of Cl, F
๐ SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Mixtures consisting of five equivalents each of borane.methyl sulfide and boron trifluoride etherate per equivalent of acetal or five equivalents of various amine-borane complexes and 10 equivalents of boron trifluoride etherate readily accomplished reductive cleavage of the glycosidic linkages of s
Reaction of the tricyclic epoxides (la) and (lb) with boron trifluoride etherate leads to fluorohydrins (2a) and (2v derived in the novel fluoride transfer, whereas (lc) undergoes isomerizationto Spiro ketone (3).