HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528600Generated: November 2, 2026
Diethyl Carbonate → Ethyl 2-(4-broMopyridin-2-yl)acetate
https://huagongshe.com/reaction/1528600
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 4-Bromo-2-methylpyridine | HCID 2762835 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(4-broMopyridin-2-yl)acetate | HCID 53419398 | — |
Reaction Steps
Lithium diisopropylamide (2 mol/L in tetrahydrofuran/heptane/ethylbenzene, 3.00 mL) was added to a solution of 4-bromo-2-methylpyridine (2.00 g) and diethyl carbonate (1.8 mL) in tetrahydrofuran (30 mL) cooled to −70° C. The solution was stirred for 1 h prior to the addition of another portion of lithium diisopropylamide (2 mol/L in tetrahydrofuran/heptane/ethylbenzene, 3.00 mL). Stirring was continued at −70° C. for one more hour and then the reaction was quenched by the addition of water. The resulting mixture was extracted with ethyl acetate and the combined extracts were washed with brine and dried (Na2SO4). The solvent was evaporated and the residue was chromatographed on silica gel (cyclohexane/ethyl acetate 95:5→1:1) to give the title compound. Yield: 2.35 g (83% of theory); LC (method 3): tR=2.86 min; Mass spectrum (ESI+): m/z=244/246 (Br) [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09090605B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-1c34bf2c51354f6f8072399987444e41 |
|---|
| Source note | uspto-grants-2015_07 |
|---|