Reactions · Wikipedia: Category:Name reactions
Hass–Bender oxidation
Oxidation
Overview
In organic chemistry, the Hass–Bender oxidation (also called the Hass–Bender carbonyl synthesis) is an organic oxidation reaction that converts benzyl halides into benzaldehydes using the sodium salt of 2-nitropropane as the oxidant. This name reaction is named for Henry B. Hass and Myron L. Bender, who first reported it in 1949.
Actions
- This entry doesn't have stoichiometric equivalents on file yet — the Reaction Scale Calculator needs at least one participant tagged with an equivalents value.
- Mechanism / source ↗
- View as JSON ↗
Search literature
More Oxidation reactions
- 2-Iodoxy-5-Methylbenzenesulfonic Acid-Catalyzed Selective Oxidation of 4-Bromobenzyl Alcohol to 4-Bromobenzaldehyde or 4-Bromobenzoic Acid with Oxone Oxidation
- A GENERAL SYNTHETIC METHOD FOR THE OXIDATION OF PRIMARY ALCOHOLS TO ALDEHYDES: (S)-(+)-2-METHYLBUTANAL (Butanal, 2-methyl-, (S)-) Oxidation
- Air Oxidation of Primary Alcohols Catalyzed by Copper(I)/TEMPO. Preparation of 2-Amino-5-bromobenzaldehyde Oxidation
- Albright–Goldman oxidation Oxidation
- ALDEHYDES BY OXIDATION OF TERMINAL OLEFINS WITH CHROMYL CHLORIDE: 2,4,4-TRIMETHYLPENTANAL (Pentanal, 2,4,4-trimethyl-) Oxidation
- ALDEHYDES FROM PRIMARY ALCOHOLS BY OXIDATION WITH CHROMIUM TRIOXIDE: HEPTANAL Oxidation