HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177057Generated: October 26, 2026
Acetic Acid → 2-(4-Chlorophenyl)-2-oxoethyl acetate
https://huagongshe.com/reaction/2177057
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(2-Bromo-4-chlorophenyl)ethanone | HCID 4712644 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(4-Chlorophenyl)-2-oxoethyl acetate | HCID 587254 | 90.1% |
Reaction Steps
To a cooled (4° C.) and stirred solution of 2-bromo-4-chloroacetophenone (5.0 g, 21.41 mmol) and glacial acetic acid (2.8 mL, 49.25 mmol) in acetonitrile was added triethylamine (6.1 mL, 44.97 mmol). The reaction mixture was warmed to room temperature, than refluxed for 3 hours. The reaction mixture was extracted with ether, acetate, washed with 1N hydrochloric acid, brine, dried, and concentrated to yield 4.1 g of acetic acid 2-(4-chlorophenyl)-2-oxo-ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09067897B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-254c1c65fedf4bc7b980642b38967d0e |
|---|
| Source note | uspto-grants-2015_06 |
|---|