HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-(5-bromopyridin-3-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-(5-Bromopyridin-3-yl)acetic acid | HCID 2802539 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | Ethyl 2-(5-bromopyridin-3-yl)acetate | HCID 54116619 | — |
Reaction Steps
15 drops of concentrated sulfuric acid are added to 5.0 g (23.1 mmol) of (5-bromopyridin-3-yl)acetic acid in 30 ml of ethanol, and the mixture is heated under reflux for 16 h. After cooling to RT, the mixture is concentrated under reduced pressure and the residue is taken up in ethyl acetate and washed with semiconcentrated sodium bicarbonate solution. The organic phase is dried over sodium sulfate, filtered and concentrated under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609698B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-2372085b2410441f991f2c113a5b69e0 |
| Source note | uspto-grants-2013_12 |