HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → methyl 3-(benzyloxy)-2-thiophenecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Hydroxy-thiophene-2-carboxylic acid methyl ester | HCID 581127 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | methyl 3-(benzyloxy)-2-thiophenecarboxylate | HCID 2764114 | 100.8% |
Reaction Steps
A mixture of methyl 3-hydroxy-2-thiophenecarboxylate (5.00 g, 31.61 mmol), benzyl bromide (3.76 mL, 31.61 mmol), and K2CO3 (4.81 g, 34.77 g) in acetone (50 mL) was stirred at reflux for 1.5 hrs. After cooled to room temperature, the mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=15/1 to 9/1) to give methyl 3-(benzyloxy)-2-thiophenecarboxylate as a pale yellow oil (7.91 g, yield: quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562811B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-75cf4f4eec564476b9452795719d4ce0 |
| Source note | uspto-grants-2003_05 |