HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Oxalate → HCID 136007385, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-Chloro-4-methyl-5-nitropyridine | HCID 345364 | — |
| Product | HCID 136007385 | HCID 136007385 | 133.2% |
Reaction Steps
A mixture of 1.5 g (8.7 mmol) 2-chloro-4-methyl-5-nitropyridine (commercially available) in 5.88 mL (43.5 mmol) diethyl oxalate was treated with 2.34 ml (15.6 mmol) 1,8-diazabicylo[5.4.0]undec-7-ene and stirred for 4 h at room temperature. After evaporation of all volatiles the residue was acidified with 1N KHSO4 aq. and extracted with DCM. The combined organic layers were dried with MgSO4 and concentrated under reduced pressure to afford 3.16 g of the title compounds which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07348323B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-d6d3546d70df421eaa5e2245fbb8cf0c |
| Source note | uspto-grants-2008_03 |