HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl malonate → 2-(4-Bromo-pyridin-2-ylmethyl)-malonic acid dimethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromo-2-(chloromethyl)pyridine | HCID 53302022 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Bromo-pyridin-2-ylmethyl)-malonic acid dimethyl ester | HCID 68385890 | 57% |
Reaction Steps
To a solution of dimethyl malonate (3.83 g) in dry THF (10 mL) at 0° C. was added NaH (463 mg) and the reaction mixture was stirred at rt for 30 min. A solution of 4-bromo-2-chloromethyl-pyridine (1.99 g) in dry THF (10 mL) was added and the reaction mixture stirred at rt for 15 h. It was then diluted with DCM, treated with a sat. aq. NH4Cl solution and the org. layers were washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The title compound was obtained, after purification by CC (Hept/EA 100:0 to 50:50), as a yellow oil (1.65 g; 57% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889676B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-df256ccca2b5409183cecbd8d86998eb |
| Source note | uspto-grants-2014_11 |