Reduction of carboxylic acids into alcohols using NaBH < inf > 4 < /inf > in the presence of catechol and/or CF < inf > 3 < /inf > COOH

dc.contributor.author Suseela, Yantrapragada
dc.contributor.author Periasamy, Mariappan
dc.date.accessioned 2022-03-27T09:12:14Z
dc.date.available 2022-03-27T09:12:14Z
dc.date.issued 1992-01-01
dc.description.abstract Reaction of aliphatic carboxylic acids (1 eq) using NaBH4 (2 eq) and catechol (2 eq) in THF at 25°C gives the corresponding alcohols in 47-49% yield besides the unreacted carboxylic acids. Reduction of aliphatic carboxylic acids (1 eq) using NaBH4 (2 eq), catechol (2 eq) and CF3COOH (1 eq) gives the aliphatic alcohols in 87-94% yields. Reductions using aliphatic acids (1 eq), NaBH4 (1 eq) and CF3COOH (1 eq) also give aliphatic alcohols in 93-95% yields. Under these conditions, the aromatic acids give poor yields. However, capric acid (1 eq) is selectively reduced to 1-decanol in 72% yield in the presence of benzoic acid (1 eq). © 1992.
dc.identifier.citation Tetrahedron. v.48(2)
dc.identifier.issn 00404020
dc.identifier.uri 10.1016/S0040-4020(01)88148-5
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040402001881485
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12579
dc.title Reduction of carboxylic acids into alcohols using NaBH < inf > 4 < /inf > in the presence of catechol and/or CF < inf > 3 < /inf > COOH
dc.type Journal. Article
dspace.entity.type
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