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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinimideHCID 11439—
ReactantN-bromobutanimideHCID 67184—
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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914128
Source datasetuspto-grants-1990_04
ORD IDord-25f5611750dd405bbcd59a6e6da485c1
Source noteuspto-grants-1990_04