HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-(2-bromophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Bromobenzyl cyanide | HCID 29625 | — |
| Product | Ethyl 2-(2-bromophenyl)acetate | HCID 2780092 | — |
Reaction Steps
To a cooled solution of 730.0 g of o-bromophenylacetonitrile in 2.9 l of absolute ethanol is added, dropwise, while stirring, 740 ml of concentrated sulphuric acid. The addition requires about 2 hours. The reaction mixture is heated under reflux for 9 hours, poured into ice water, and extracted with 2.5 l of ether. The ether extracts are washed, dried, and concentrated. The residue is distilled to give 780.0 g of ethyl o-bromophenylacetate, bp. about 115°-117° (4mm), nD26 1,5434.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04001233 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-48355715b1c14684b929111462e6fbf1 |
| Source note | uspto-grants-1977_01 |