HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666941Generated: October 30, 2026
Diethyl Malonate → (Cyclopentylmethyl)propanedioic acid
https://huagongshe.com/reaction/1666941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | (Bromomethyl)cyclopentane | HCID 12723264 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (Cyclopentylmethyl)propanedioic acid | HCID 55250614 | 59% |
Reaction Steps
A solution of diethyl malonate (36.91 g, 230.4 mmol), anhydrous methanol (400 mL), and NaOMe (25% in methanol, 49.79 g, 230.4 mmol) is stirred at reflux for one hour under nitrogen. Bromomethyl-cyclopentane (31.31 g, 192.0 mmol) is added to the mixture, and stirred for an additional 3 hours. A solution of NaOH (23.04 g, 576.0 mmol) in water (400 mL) is added, and the mixture is stirred for an additional 1 hour at reflux. The mixture is cooled, diluted with water, and extracted with ether. The ether layer is discarded, and the aqueous layer is acidified with 1N HCl to pH=1. The aqueous layer is extracted with EtOAc. The EtOAc layers are combined, dried over Na2SO4, and concentrated. This gives 2-cyclopentylmethyl-malonic acid (21.0 g, 59% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08044199B2 |
|---|
| Source dataset | uspto-grants-2011_10 |
|---|
| ORD ID | ord-38d86fefef784c2ba60afdd9fee24131 |
|---|
| Source note | uspto-grants-2011_10 |
|---|