HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 2-(4-Chlorocarbonylphenyl)-2-methylpropionic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Methyl 2-methyl-2-phenylpropanoate | HCID 143498 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Chlorocarbonylphenyl)-2-methylpropionic acid methyl ester | HCID 25111212 | — |
Reaction Steps
To a suspension of AlCl3 (500.0 mg, 3.75 mmol) in CH2Cl2 at −10° C. was added dropwise oxalyl chloride (476.0 mg, 3.75 mmol) in CH2Cl2. The mixture was stirred at this temperature for 30 min. Then a solution of 2-methyl-2-phenyl-propionic acid methyl ester (178.0 mg, 1.0 mmol) in CH2Cl2 was added. The resulted mixture was stirred at −10° C. for 1 hr and rt overnight. The mixture was filtered through a pad of celite, the solvent and excess oxalyl chloride was removed under reduced pressure. The residue was dissolved in chlorobenzene and refluxed for 4 hr. Solvent was removed and the residue was dried to give 2-(4-chlorocarbonyl-phenyl)-2-methyl-propionic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07312214B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-1ae7008a1fbb46c28dc5fd0759be2053 |
| Source note | uspto-grants-2007_12 |