HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 54349507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 15132295 | HCID 15132295 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54349507 | HCID 54349507 | — |
Reaction Steps
A mixture of 4-(1-ketotridecyl)-2-trimethylsilylfuran (Compound 26, 84.5 mg, 0.25 mmol), zinc (100 mg, 1.53 mmol) and ethyl bromoacetate (105 mg, 0.63 mmol) in benzene (6 ml) was refluxed for 2 hours. After cooling to 0°, acetic anhydride (83 ul, 0.88 mmol) was added. Stirring was continued for 14 hours while the cooling bath attained room temperature. The mixture was washed with 5% sodium bicarbonate and water. Evaporation of the dried (magnesium sulfate) organic phase gave a residue which was purified by a silica column using 2% ethyl ether/hexane to give the title ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05013850 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-13b0975b9c3b4cd2ad51ec7c7786714b |
| Source note | uspto-grants-1991_05 |