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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378527Generated: October 26, 2026

Ethanol → 2-Methyl-2-butanol

https://huagongshe.com/reaction/378527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethanolHCID 887—
Reactant1-PropanolHCID 1031—
ReactantIsopropanolHCID 3776—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Solvent(+-)-2-ButanolHCID 6568—
Product2-Methyl-2-butanolHCID 6405—
ProductMethacroleinHCID 6562—

Reaction Steps

In order to take advantage of the combustion step, the naphthalate diester is selected to produce an appropriate alcohol byproduct that has a volatility comparable to or greater than that of water. There are several ways of expressing this selection. As a first, the naphthalene diester can be selected on the basis of being one that will produce an alcohol byproduct that is selected form the group consisting of methanol (CH3OH, b.p. 64.5° C.), ethanol (CH3CH2OH; b.p. 64.5° C.), propanol (CH3CH2CH3OH; b.p. 78.3° C.), and isopropanol (CH3CHOHCH3 ; 82.5° C.), all of which have boiling points less than that of water and thus the appropriate volatility. Other possible alcohol byproducts that define qualifying naphthalene diesters, include secondary butanol (CH3CH2CHOHCH3 ; b.p. 99.5° C.) and tertbutanol ((CH3)3COH; b.p. 83° C.). Naphthalene diesters that produce isobutenal ((CH3)2CHCH2OH; b.p. 108° C.) and tertpentanol (CH3CH2C(OH)(CH3)2 ; b.p. 102° C.) are also candidates although their boiling points slightly exceed that of water at atmospheric pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06031065
Source datasetuspto-grants-2000_02
ORD IDord-b2bf3a292f2a4af1902ab667dcc558a3
Source noteuspto-grants-2000_02