HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 19917140, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Thiophene-3-methanol | HCID 123570 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19917140 | HCID 19917140 | — |
Reaction Steps
1.0 g of 3-thiophenemethanol was dissolved in 6 ml of dimethylformamide, and under ice cooling, 0.36 g of 60% oily sodium hydride and 1 ml of ethyl bromoacetate were added. The mixture was stirred at room temperature for 15 hours, and then worked up in a customary manner. The product was purified by silica gel column chromatography [hexane/ethyl acetate=6/1] to give 0.9 g of ethyl 3-thienylmethoxyacetate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05439932 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-dba3ff5e4797434dac60d81498edeee6 |
| Source note | uspto-grants-1995_08 |