HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 5-Chloro-2-propoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Chloro-2-hydroxybenzamide | HCID 348094 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-Chloro-2-propoxybenzamide | HCID 9452884 | — |
Reaction Steps
A stirred mixture of 5-chloro-2-hydroxybenzamide (20 g), 1-bromopropane (13.4 ml), potassium iodide (2.49 g) and anhydrous potassium carbonate (24.15 g) in acetone (250 ml) was heated under reflux for 20 hours. The cooled reaction mixture was filtered and the filter cake was washed with acetone. The filtrate and washings were combined and evaporated under reduced pressure to yield a residue which was washed with water, dilute aqueous sodium hydroxide, water and with diethyl ether to yield a crude product (19.85 g). This was recrystallised from acetonitrile, partitioned between chloroform and dilute aqueous sodium hydroxide, and was recrystallised from ethanol to yield 5-chloro-2-propoxybenzamide (16.78 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05073559 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-28af009435194eb6bf88e957b6f73117 |
| Source note | uspto-grants-1991_12 |