HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508551Generated: November 2, 2026
beta-(p-Chlorophenyl)propionic acid → Methyl 3-(4-chlorophenyl)propanoate
https://huagongshe.com/reaction/1508551
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | beta-(p-Chlorophenyl)propionic acid | HCID 123137 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 3-(4-chlorophenyl)propanoate | HCID 8027172 | — |
Reaction Steps
To a solution of 3-(4-chlorophenyl)propionic acid (2.45 g, 13.27 mmol) in toluene (65 mL) and methanol (10 mL) was added trimethylsilyldiazomethane (2M solution in hexane, 7.63 mL, 15.26 mmol). The mixture was allowed to stir for 1 hour and gas evolution was observed initially. After 1 hour, the mixture became homogeneous and was quenched via addition of 3.5 mL of acetic acid. The mixture was concentrated in vacuo, and purified via column chromatography on a Biotage 65i column eluting with 0% ethyl acetate in hexanes (1 CV) followed by a gradient to 50% ethyl acetate in hexanes (over 7 CV) to furnish the desired product. 1H NMR (CDCl3, 500 MHz) δ 7.25 (d, J=8.2 Hz, 2H), 7.13 (d, J=8.3 Hz, 2H), 3.67 (s, 3H), 2.92 (t, J=7.7 Hz, 2H), 2.61 (t, J=7.7 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09221834B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-711497d7fa234d88ba0341118ba2ac94 |
|---|
| Source note | uspto-grants-2015_12 |
|---|