HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072706Generated: October 30, 2026
Succinimide → Methyl 2-[2-(bromomethyl)phenyl]-3-methoxyprop-2-enoate
https://huagongshe.com/reaction/2072706
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Succinimide | HCID 11439 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| 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 N-bromosuccinimide, 0.2 g of azobisisobutyronitrile and 150 ml of CCl4 are slowly heated to 90° C. and kept at this temperature until all of 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 |
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| Patent number | US04914128 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-25f5611750dd405bbcd59a6e6da485c1 |
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| Source note | uspto-grants-1990_04 |
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