HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 5-Carboethoxythiophen-2-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-(Ethoxycarbonyl)thiophene-2-carboxylic acid | HCID 15232123 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Carboethoxythiophen-2-carbonyl chloride | HCID 10262858 | — |
Reaction Steps
To a suspension of acid 35 (0.64 g, 3.2 mmol) in dichloromethane (20 mL) under argon at room temperature was added a 2.0M solution of (COCl)2 in dichloromethane (2.4 mL, 4.8 mmol) and two drops of DMF, and stirred overnight. Excess (COCl)2 and dichloromethane were removed at reduced pressure, and the viscous, light, yellow product was dried overnight to afford the desired benzoyl chloride 36 as a yellow solid. The structure of the product was also confirmed using IR and 1H NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05466861 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-144f394f694e440780ac1145e4894bb7 |
| Source note | uspto-grants-1995_11 |