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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807022Generated: November 1, 2026

3-Methyl-3-(5-methyl-furan-2-yl)-butyric acid methyl ester → 3-Methyl-3-(5-methyl-furan-2-yl)-butan-1-ol

https://huagongshe.com/reaction/1807022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-3-(5-methyl-furan-2-yl)-butyric acid methyl esterHCID 14357291—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-3-(5-methyl-furan-2-yl)-butan-1-olHCID 1496150891.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Step D To a solution of 3-methyl-3-(5-methyl-furan-2-yl)-butyric acid methyl ester (1.5 g, 7.8 mmol) in anhydrous tetrahydrofuran (50 mL) at 0° C. was added a tetrahydrofuran solution (1 M) of LiAlH4 (10 mL, 10 mmol) under nitrogen. The reaction mixture was stirred at 0° C. for 1 h, then poured into a ice-water. The mixture was extracted with ethyl acetate. The organic layer were separated, washed with water, aqueous HCl solution, brine, dried over MgSO4, and concentrated to give 3-methyl-3-(5-methyl-furan-2-yl)-butan-1-ol as a yellow oil (1.2 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-c8ef4063fadc4bba819f15fdfb1f6086
Source noteuspto-grants-2013_01