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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21846Generated: October 25, 2026

Hydrochloric Acid → 4-Acetoxy-2-methyl-2-buten-1-ol

https://huagongshe.com/reaction/21846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Acetoxy-2-methyl-2-buten-1-ol formateHCID 54335244—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product4-Acetoxy-2-methyl-2-buten-1-olHCID 53822297.7%

Reaction Steps

Sodium bicarbonate (0.40 g, 4.75 mmol, 10 mol %) was added to a solution of 4-acetoxy-2-methyl-2-buten-1-ol formate (8.18 g, 47.5 mmol) in methanol (40 ml). The mixture was stirred at room temperature for 2 hours. After completion of the reaction, most of the methanol was evaporated under reduced pressure. The resulting reaction mixture was poured into a mixture of ice-cooled water (20 ml) and ethyl acetate (100 ml). The pH of the aqueous layer was adjusted to 5 to 6 with 1N hydrochloric acid, and the ethyl acetate layer was separated. The aqueous layer was extracted with ethyl acetate (50 ml) twice. The ethyl acetate layers were combined and dried over anhydrous sodium sulfate. Evaporation of the ethyl acetate gave 4-acetoxy-2-methyl-2-buten-1-ol (6.69 g, 46.4 mmol; Yield: 97.7%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424478
Source datasetuspto-grants-1995_06
ORD IDord-e443ffc7c83743028b9c10548e7baa67
Source noteuspto-grants-1995_06