HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502942Generated: November 4, 2026
Hydrochloric Acid → (3-Chloro-4-methylthiophen-2-yl)methanol
https://huagongshe.com/reaction/502942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 3-chloro-4-methylthiophene-2-carboxylate | HCID 2777567 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Chloro-4-methylthiophen-2-yl)methanol | HCID 59767697 | 92.4% |
Reaction Steps
Lithium aluminum hydride (1.35 g) was added to a THF (50 ml) solution of methyl 3-chloro-4-methylthiophene-2-carboxylate (3.40 g) at 0° C., followed by stirring at 0° C. for 20 minutes. An 1M aqueous hydrochloric acid solution was added to the reaction solution and the whole was stirred at room temperature for 1 hour. The solution was filtered and, after ethyl acetate was added, the organic layer was separated. Furthermore, the organic layer washed with brine and, after drying over anhydrous sodium sulfate and filtration, the solvent was removed by evaporation under reduced pressure. The resulting crude product was purified by column chromatography (hexane:ethyl acetate=4:1) to obtain 2.68 g of (3-chloro-4-methyl-2-thienyl)methanol (pale yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07776897B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-10c891dbc6f84eb99077cbf9ea87afca |
|---|
| Source note | uspto-grants-2010_08 |
|---|