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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877255Generated: October 26, 2026

Water → 5-(1,3-Dioxolan-2-yl)-2-ethylthiophene-3-carbaldehyde

https://huagongshe.com/reaction/1877255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 5-(1,3-dioxolan-2-yl)-2-ethylthiophene-3-carboxylateHCID 68509635—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product5-(1,3-Dioxolan-2-yl)-2-ethylthiophene-3-carbaldehydeHCID 8664639688.2%

Reaction Steps

To a solution of ethyl 5-(1,3-dioxolan-2-yl)-2-ethylthiophene-3-carboxylate (8.71 g) synthesized above in tetrahydrofuran (170 mL) was added lithium aluminum hydride (2.58 g) at 0° C., and the mixture was stirred for 1 hr. Water (5.20 mL) was added to quench the reaction, 1N aqueous sodium hydroxide solution (5.20 mL) was added, and the mixture was stirred at room temperature for 1 hr. The resulting insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give a colorless oil. To a solution of the obtained oil in tetrahydrofuran (150 mL) was added activated manganese dioxide (36.0 g), and the mixture was stirred at room temperature for 4.5 hr. Manganese dioxide was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (6.36 g, 88%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-8437ab8f44c34e53a43f661fa92b586c
Source noteuspto-grants-2012_11