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Study of l-phenylacetylcarbinol. VII

Š. Bauer, L. Masler, and Š. Országh

Slovak Academy of Sciences, Bratislava

 

Abstract: cf. C.A. 53, 3125i. l-PhCH(OH)Ac (I) boiled with Ac2O and acetylated with AcCl in C5H5N gives the optically active Ac ester, b11 140-1°, 139-40°, [α]20D -211.8 ± 4° (c 4.1, EtOH), -209.7 ± 4° (c 4, EtOH), n20D 1.5064, 1.5063. Benzoylation of I with BzCl in C5H5N yields an optically active Bz ester, m. 49-51°, [α]20D -145.5 ± 4° (c 4.6, EtOH). No isomerization occurs during esterification of I. An optically active Me ether of I, m. 107-9°, [α]20D -145.54° (c 4.6, EtOH) was also prepd.

Full paper in Portable Document Format: 1211a639.pdf (in Slovak)

 

Chemical Papers 12 (11) 639–641 (1958)

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