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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinimideHCID 11439—
ReactantBromosuccinimideHCID 38309—
ReactantMethyl 3-methoxy-2-o-tolylacrylateHCID 435882—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 2-[2-(bromomethyl)phenyl]-3-methoxyprop-2-enoateHCID 5339534997.3%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782177
Source datasetuspto-grants-1988_11
ORD IDord-735ddd122fda43d1881459ab87a1dbef
Source noteuspto-grants-1988_11