HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 2-(4-Chloro-2-methoxycarbonyl-phenyl)-2-bromo-acetic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Chloro-2-methoxycarbonyl-phenyl acetic acid methyl ester | HCID 12899655 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(4-Chloro-2-methoxycarbonyl-phenyl)-2-bromo-acetic acid methyl ester | HCID 86722271 | 120.8% |
Reaction Steps
18E (16.48 mmol) was dissolved in CCl4 (50 mL), and was added NBS (N-bromosuccinimide, 3.23 g, 18.13 mmol), followed by catalytic amount of BPO (benzoyl peroxide). The reaction mixture was refluxed for about 20 hours under stirring. When no more product was produced any more, the reaction mixture was cooled and filtered. To the filtrate was added NBS (1.6 g, 8.24 mmol) and catalytic amount of BPO. The reaction mixture was refluxed for additional 10 hours. After the reaction completed, the mixture was cooled and filtered. The filtrate was concentrated to give 6.4 g of a crude product (19A), which was used directly for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969373B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-cfb59e5d069f4e4f98143453397b206c |
| Source note | uspto-grants-2015_03 |