HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272264Generated: October 31, 2026
Dimethylformamide → 3,5-Diisopropyl salicylamide
https://huagongshe.com/reaction/1272264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3,5-Diisopropylsalicylic acid | HCID 30543 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Product | 3,5-Diisopropyl salicylamide | HCID 18456902 | 40% |
Reaction Steps
To a solution of 3,5-diisopropylsalicylic acid (Aldrich) (10 mmole, 2.2 g) and dichloromethane (20 mL), oxalyl-chloride (Merck) (11.0 mmole, 1.03 mL) and DMF (Aldrich) (80 μL) were added. The reaction mixture was refluxed for 1 hour, whereupon the solvent and the excess of oxalyl-chloride were removed under reduced pressure. The obtained oily product was dissolved in dichloromethane (50 mL) and ammonia gas was introduced into reaction mixture under cooling. The solution was diluted with water and, after drying with sodium sulfate, the organic layer was evaporated under reduced pressure. A yellow residue was recrysatallized from n-hexane, whereat there were obtained 876 mg (40%) of 3,5-diisopropyl salicylamide in the form of a white crystalline product:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07208518B2 |
|---|
| Source dataset | uspto-grants-2007_04 |
|---|
| ORD ID | ord-b34348152e9d47119d1b4899d5d6788c |
|---|
| Source note | uspto-grants-2007_04 |
|---|