The Journal of Organic Chemistry

Selective reduction of carboxylic acids into alcohols using sodium borohydride and iodine

JVB Kanth, M Periasamy

Index: Kanth, J. V. Bhaskar; Periasamy, Mariappan Journal of Organic Chemistry, 1991 , vol. 56, # 20 p. 5964 - 5965

Full Text: HTML

Citation Number: 164

Abstract

General Procedure for Reduction. A solution of the carboxylic acid (10 mmol) in THF (20 mL) was slowly added to a suspension of NaBHl (12 mmol) in THF (20 mL) at room tem-Derature (10 mid. The mixture was stirred until evolution of gas min) at the temperature mentioned in Table I. Additional hydrogen evolved. The contents were further stirred for 1 h. Dilute HCl (5 mL, 3 N) was added carefully and the mixture extracted with ether. The combined ether ...

Related Articles:

Practical and Chemoselective Reduction of Acyl Chloride to Alcohol by Borohydride in Aqueous Dichloromethane

[Rajan, Ramya; Badgujar, Sachin; Kaur, Kamaljit; Malpani, Yashwardhan; Kanjilal, Pranab R. Synthetic Communications, 2010 , vol. 40, # 19 p. 2897 - 2907]

Electrochemical reduction of methyl 2-bromomethylbenzoate at carbon cathodes in dimethylformamide containing water

[Allen, Caroline R.; Brown, Drew K.; Potts, Jessica L.; Ji, Chang Journal of the Electrochemical Society, 2013 , vol. 160, # 7 p. G3069-G3072]

Preparation of 1-ethoxyisobenzofuran. Mechanistic aspects of the Meerwein ortho-ester reaction

[Mir-Mohamad-Sadeghy, Bagher; Rickborn, Bruce Journal of Organic Chemistry, 1984 , vol. 49, # 9 p. 1477 - 1481]

More Articles...