Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071872Generated: October 30, 2026

Water → 2,3-Dihydro-3,3-dimethyl-2-(3-methylbutoxy)-5-benzofuranyl methanesulphonate

https://huagongshe.com/reaction/2071872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsoamyl AlcoholHCID 31260—
Reactant(2-Hydroxy-3,3-dimethyl-2H-1-benzofuran-5-yl) methanesulfonateHCID 536079—
CatalystSulfuric AcidHCID 1118—
SolventBenzeneHCID 241—
Product2,3-Dihydro-3,3-dimethyl-2-(3-methylbutoxy)-5-benzofuranyl methanesulphonateHCID 2140955886%

Reaction Steps

A mixture of 2,3-dihydro-3,3-dimethyl-2-hydroxybenzofuran-5-yl methanesulphonate (13g, 0.05 mole), 3-methyl-1-butanol (4.4g, 0.05 mole) and concentrated sulphuric acid (4 drops) in benzene (50 ml) was heated at reflux under a Dean and Stark trap until 0.9 ml water (0.05 mole) had been eliminated. The reaction mixture was cooled, washed with dilute aqueous sodium hydroxide solution and with water (twice) and dried over sodium sulphate. The benzene was then distilled off under reduced pressure to give 2,3-dihydro-3,3-dimethyl-2-(3-methylbutoxy)-5-benzofuranyl methanesulphonate as a yellow oil (14 g, 86% yield) which slowly solidified (melting point 35°-38° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049420
Source datasetuspto-grants-1977_09
ORD IDord-2a2c97a73a3c4fdeaacc03cf186c59c9
Source noteuspto-grants-1977_09