HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523349Generated: October 31, 2026
Diethyl Oxalate → HCID 55269669, compound
https://huagongshe.com/reaction/523349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Cyclohexane, 1-bromo-4-methyl- | HCID 22727 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 55269669 | HCID 55269669 | 76% |
Reaction Steps
A Grignard reagent prepared from 1-bromo-4-methylcyclohexane (20.0 g, 0.11 mol) and magnesium (2.9 g, 0.12 mol) in THF (110 ml) was added dropwise (during a period of 80 min) to a mechanically stirred solution of diethyl oxalate (16.0 g, 0.11 mol) in THF (250 ml) at −78° C. The mixture was left stirring for 2 h and then slowly warmed up to 0° C. A saturated solution of NH4Cl (100 ml) was added and the formation of a white precipitate was observed. Extraction with diethyl ether (2×), washing with water, drying (Na2SO4) and concentrating afforded 22.6 g of the crude compound. Kugelrohr distillation of 10 g (100° C./2 mbar) gave 7.74 g (76%) of ethyl 2-(4-methylcyclohexyl)-2-oxoacetate as a slightly yellow oil (mixture of cis/trans isomers ca. 1:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09334464B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-7da4b458dda94b05af531863fd9432a0 |
|---|
| Source note | uspto-grants-2016_05 |
|---|