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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605693Generated: October 29, 2026

Iodine → 2-Propenoic acid, 3-(2-aminophenyl)-, ethyl ester, (2E)-

https://huagongshe.com/reaction/1605693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantDiethyl EtherHCID 3283—
ReactantMethyl iodideHCID 6328—
ReactantEthyl cyanoacetateHCID 7764—
ReactantBromobenzeneHCID 7961—
ReactantMagnesiumHCID 5462224—
Product2-Propenoic acid, 3-(2-aminophenyl)-, ethyl ester, (2E)-HCID 2749050—

Reaction Steps

To a solution of dry ethyl ether (300 ml.) is added magnesium turnings (16.9 g.). Bromobenzene (103 g.) in ether (600 ml.) is added at a rate to maintain gentle refluxing (An iodine crystal or a ml. of methyliodide often must be added to initiate the reaction.). Refluxing is continued until most of the magnesium has reacted. Ethyl cyanoacetate (30 g.) is added over a 30 minute period and the reaction mixture allowed to stir for 3 hours at room temperature after which time 3.5N sulfuric acid (180 ml.) is added and the reaction allowed to stir for 30 additional minutes. The aqueous layer is extracted with diethyl ether and the organic layer washed with water and dried over sodium sulfate. Removal of the ether in vacuo followed by distillation of the residual oil gives the desired product, b.p. at 0.4 mm, 138°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950525
Source datasetuspto-grants-1976_04
ORD IDord-b91465bdf90443509102eb21b5be17b8
Source noteuspto-grants-1976_04