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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066692Generated: October 26, 2026

Butanal → 2-(1-Hydroxybutyl)-2-methyl-1,3-dithian

https://huagongshe.com/reaction/1066692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanalHCID 261—
ReactantWaterHCID 962—
Reactant2-Methyl-1,3-dithianeHCID 22329—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-(1-Hydroxybutyl)-2-methyl-1,3-dithianHCID 12476960—

Reaction Conditions

Temperature-30 °C

Reaction Steps

56 mmol of n-butyllithium (35 ml of a 1.6 M solution in hexane) were added with stirring to a solution of 2-methyl-1,3-dithian (7 g, 52.1 mmol) in 100 ml of dry tetrahydrofuran at −30° C. under argon. After stirring at −30° C. for 2 hours, the mixture was cooled to −78° C. 4.2 g (58.3 mmol) of freshly distilled n-butyraldehyde were added dropwise in the course of 15 minutes and the mixture was stirred for a further 30 minutes. After warming to 20° C., it was poured into a beaker containing 300 ml of water and 100 ml of n-hexane. The organic phase was separated off and the aqueous phase was extracted three times with 50 ml of dichloromethane in each case. The combined organic phases were washed with 10% strength by weight potassium hydroxide solution, water and concentrated sodium chloride solution, dried over anhydrous sodium sulfate and then distilled. 8.82 g of 2-(1-hydroxybutyl)-2-methyl-1,3-dithian were isolated as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245328B1
Source datasetuspto-grants-2001_06
ORD IDord-4a3edc1b5e0642e8be21e20e3154a1ca
Source noteuspto-grants-2001_06