HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231405Generated: November 2, 2026
Succinimide → Methyl 2-[2-(bromomethyl)phenyl]-3-methoxyprop-2-enoate
https://huagongshe.com/reaction/2231405
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Succinimide | HCID 11439 | — |
| Reactant | Bromosuccinimide | HCID 38309 | — |
| Reactant | Methyl 3-methoxy-2-o-tolylacrylate | HCID 435882 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 2-[2-(bromomethyl)phenyl]-3-methoxyprop-2-enoate | HCID 53395349 | 97.3% |
Reaction Steps
20.6 g of the methyl α-(2-methylphenyl)-β-methoxyacrylate obtained as described in Method A, 17.65 g of bromosuccinimide, 0.2 g of azobisisobutyronitrile and 150 ml of CCl4 are slowly heated to 90° C. and kept at this temperature until all the succinimide floats on the solvent. The mixture is filtered, the filtrate is evaporated down, the remaining oil is dissolved in about 5 ml of acetone and the solution is brought to crystallization with n-hexane. 27.5 g of colorless crystals of melting point 86°-87° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04782177 |
|---|
| Source dataset | uspto-grants-1988_11 |
|---|
| ORD ID | ord-735ddd122fda43d1881459ab87a1dbef |
|---|
| Source note | uspto-grants-1988_11 |
|---|