HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860125Generated: November 1, 2026
Methanol → 2-(4-Bromo-phenyl)-3-cyclopentyl-propionic acid methyl ester
https://huagongshe.com/reaction/1860125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-(4-Bromo-phenyl)-3-cyclopentyl-propionic acid | HCID 22315094 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | 2-(4-Bromo-phenyl)-3-cyclopentyl-propionic acid methyl ester | HCID 46221157 | 97% |
Reaction Steps
A solution of 2-(4-bromo-phenyl)-3-cyclopentyl-propionic acid (1.37 g, 4.61 mmol) in methanol (23 mL) was treated slowly with 5 drops of concentrated sulfuric acid. The resulting reaction mixture was heated under reflux for 42 h. The reaction mixture was allowed to cool to 25° C. and then concentrated in vacuo to remove methanol. The residue was diluted with ethyl acetate (200 mL). The organic phase was washed with a saturated aqueous sodium bicarbonate solution (1×100 mL), washed with a saturated aqueous sodium chloride solution (1×100 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 19/1 hexanes/ethyl acetate) afforded 2-(4-bromo-phenyl)-3-cyclopentyl-propionic acid methyl ester (1.40 g, 97%) as a light yellow oil: EI-HRMS m/e calcd for C15H19BrO2 (M+) 310.0568, found 310.0569.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06528543B1 |
|---|
| Source dataset | uspto-grants-2003_03 |
|---|
| ORD ID | ord-1b10af1962a94ac58d60289e7b48c075 |
|---|
| Source note | uspto-grants-2003_03 |
|---|