HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-Chloro-5-methylthiophene-2-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Chloro-5-methylthiophene-2-carboxylic acid | HCID 16640001 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Chloro-5-methylthiophene-2-carbonyl chloride | HCID 18376862 | 101% |
Reaction Steps
To a suspension of 2-carboxy-3-chloro-5-methylthiophene (1.2 g, 6.6 mmol) in methylene chloride (16 mL) at 0° C. were added oxalyl chloride (0.6 mL, 7.3 mmol) and a drop of DMF. The mixture was stirred at ambient temperature for 5 hours, then concentrated of all volatiles and dried in vacuo to afford 1.3 g (quantitative yield) of 2-chlorocarbonyl-3-chloro-5-methylthiophene as a pale yellow solid; NMR (DMSO-d6/TFA) 7.4 (s, 1), 2.5 (s, 3) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498185B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-4b0b88dd956d4bd98fb9abbbfbe86a97 |
| Source note | uspto-grants-2002_12 |