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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Product | 2-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03950525 |
|---|
| Source dataset | uspto-grants-1976_04 |
|---|
| ORD ID | ord-b91465bdf90443509102eb21b5be17b8 |
|---|
| Source note | uspto-grants-1976_04 |
|---|