HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 5-Bromo-2-pyridinyl Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178515818 | HCID 178515818 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Bromo-2-pyridinyl Acetate | HCID 23438576 | 52% |
Reaction Steps
A suspension of 0.5 g (2.87 mmol) of 5-bromo-2-pyridinol in 10 ml of ethyl ether is prepared and 1 ml (7.1 mmol) of triethylamine and then 1 ml (14 mmol) of acetyl chloride are added at ambient temperature. The mixture is stirred at ambient temperature for 24 hours and then the insoluble materials are removed by filtration. The filtrate is concentrated under reduced pressure and the crude product is purified by chromatography on silica gel, elution being carried out using a toluene/2-propanol mixture (9/1; v/v). The expected product is obtained in the form of a pale yellow powder with a yield of 52%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08013010B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-494fc5c5a5db4fb3a27b111fd16d8f74 |
| Source note | uspto-grants-2011_09 |