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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 5-(1,3-dioxolan-2-yl)-2-ethylthiophene-3-carboxylate | HCID 68509635 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(1,3-Dioxolan-2-yl)-2-ethylthiophene-3-carbaldehyde | HCID 86646396 | 88.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08309580B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-8437ab8f44c34e53a43f661fa92b586c |
|---|
| Source note | uspto-grants-2012_11 |
|---|