HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2,2-Dimethylmalonic acid t-butyl ester cyclohexyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 3-(Tert-butoxy)-2,2-dimethyl-3-oxopropanoic acid | HCID 254415 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2,2-Dimethylmalonic acid t-butyl ester cyclohexyl ester | HCID 67469976 | — |
Reaction Steps
To a mixture of 2,2-dimethylmalonic acid mono-t-butyl ester [CAS No. 143688-40-8] (800 mg), DMAP (104 mg), and dichloromethane (8 mL), cyclohexanol (0.494 mL) and WSC (976 mg) were sequentially added at 0° C. The resulting mixture was stirred overnight at room temperature, and TBME (50 mL) was added thereto. The resulting mixture was sequentially washed with water (30 mL) and saturated aqueous sodium chloride solution (30 mL), and dried over anhydrous magnesium sulfate. The resulting mixture was filtered, and the filtrate obtained was concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography (mixed solvent of heptane-ethyl acetate) to obtain the captioned compound (817 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436009B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-fa9d8e23bd104a26acf716c18aadbbc6 |
| Source note | uspto-grants-2013_05 |