HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-(2-Chlorophenyl)-2-oxopropyl Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(3,4-Dichlorophenyl)-2-oxopropyl Acetate | HCID 16100072 | — |
| Reactant | 1-Chloro-3-(2-chlorophenyl)propan-2-one | HCID 16100205 | — |
| Product | 3-(2-Chlorophenyl)-2-oxopropyl Acetate | HCID 16100060 | 43% |
Reaction Steps
The procedure described above for the synthesis of 3-(3,4-dichlorophenyl)-2-oxopropyl acetate was followed, reacting 1-chloro-3-(2-chlorophenyl)propan-2-one (0.556 g, 2.74 mmol) with acetic acid (0.31 mL, 0.33 g, 5.5 mmol) and triethylamine (0.76 mL, 0.56 g, 5.5 mmol). Flash chromatography over silica gel (5-40% ethyl acetate in hexanes) gave pure product (0.251 g, 43% yield): 1H NMR (400 MHz, CDCl3) δ 2.17 (s, 3H) 3.88 (s, 2H) 4.75 (s, 2H) 7.24-7.27 (m, 3H) 7.38-7.42 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07465798B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-76f870d60d4c467e86f8a70115abd29e |
| Source note | uspto-grants-2008_12 |