Berger, F. M. et al. published their research in Journal of Pharmacology and Experimental Therapeutics in 1950 | CAS: 115-84-4

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Synthetic Route of C9H20O2

The anticonvulsant action of 2,2-diethyl-1,3-propanediol and some of its homologs and esters was written by Berger, F. M.;Ludwig, B. J.. And the article was included in Journal of Pharmacology and Experimental Therapeutics in 1950.Synthetic Route of C9H20O2 The following contents are mentioned in the article:

cf. C.A. 43, 8546g. 2,2-Diethyl-1,3-propanediol (I) strongly antagonizes the convulsant and lethal effects of metrazole, strychnine, and picrotoxin. These antagonistic effects occur with doses which do not exert a hypnotic or anesthetic action. I can be effectively administered enterally or parenterally. Its duration of action is short. I does not affect spinal reflexes and has little action on the spinal cord. It acts by a depressant effect on the forebrain and midbrain. I is partly conjugated in the body as an ether type glucuronide. Another portion is oxidized to α,α-diethylhydracrylic acid (II), m. 62.5°, n65D 1.4458. The further oxidation product, diethylmalonic acid (III) was not found in the urine of patients receiving I. II and III in doses of 400 mg./kg. had no anticonvulsant action. The 2,2-dimethyl, 2-methyl-2-ethyl, 2-methyl-2-propyl, 2-methyl-2-isopropyl, 2-methyl-2-butyl, 2-ethyl-2-butyl, 2-ethyl-2-phenyl, 2,2-dipropyl, and 2,2-dibutyl homologs of I showed an anticonvulsant activity of a similar order to that of I. None had a longer duration of action. I diacetate had a less intense but more prolonged action than I. I monoacetate, succinate, and dibenzoate showed no advantage over I. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Synthetic Route of C9H20O2).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Synthetic Route of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts