HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596022Generated: October 31, 2026
Diethyl Malonate → 8-Oxabicyclo[3.2.1]octane-3,3-dicarboxylic acid diethyl ester
https://huagongshe.com/reaction/1596022
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | cis-2,5-Bis(hydroxymethyl)tetrahydrofuran ditosylate | HCID 86755706 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-Oxabicyclo[3.2.1]octane-3,3-dicarboxylic acid diethyl ester | HCID 304033 | — |
Reaction Steps
Sodium hydride (2.28 grams, 95 mmole) is added in portions to a stirred solution of diethyl malonate (15 mL, 99 mmole) in N,N-dimethylformamide (400 mL). The mixture is stirred for 45 minutes at which time evolution of hydrogen is complete. A solution of cis-2,5-bis(hydroxymethyl)tetrahydrofuran ditosylate (19.0 grams, 43 mmole) in N,N-dimethylformamide (400 mL) is then added dropwise. The mixture is heated in an oil bath at 140° C. overnight. After cooling to room temperature, the mixture was quenched by addition of saturated aqueous ammonium chloride solution and concentrated under vacuum. The residual oil is taken up in water and extracted with diethyl ether. The organic extract is washed with water and brine, dried over magnesium sulfate and concentrated to an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06288246B1 |
|---|
| Source dataset | uspto-grants-2001_09 |
|---|
| ORD ID | ord-e26e461067ac4b1ea8671de89f3f983b |
|---|
| Source note | uspto-grants-2001_09 |
|---|