HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044418Generated: November 2, 2026
2-Bromo-5-chloropyridine → HCID 58580279, compound
https://huagongshe.com/reaction/1044418
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-5-chloropyridine | HCID 817098 | — |
| Reactant | HCID 178525802 | HCID 178525802 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58580279 | HCID 58580279 | 63% |
Reaction Steps
Title compound was prepared according to the procedure described in: Hasnik, Z.; Silhar, P.; Hocek, M. Synlett 2008, 4, 543. A solution of (benzoyloxymethyl)zinc(II) iodide Part B (2.17 mL, 1.949 mmol) was added to a solution of 2-bromo-5-chloropyridine (125 mg, 0.650 mmol) and Pd(PPh3)4 (37.5 mg, 0.032 mmol) in THF (1.30 mL). The reaction mixture was stirred at RT for 5 h at which point it was quenched with 1M NaH2PO4 (30 mL) The solid formed was filtered and washed well with water. The filtrate was extracted with DCM (3×25 mL) and the combined organic layers were dried over anhydrous Na2SO4 and concentrated. The crude product was subjected to flash chromatography (silica gel/hexanes-EtOAc 100:0 to 50:50 gradient) to afford (5-chloropyridin-2-yl)methyl benzoate 16C (101 mg, 63% yield) as an off-white solid. LC-MS, [M+H]+=248. HPLC-Method 8; 3.30 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08563583B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-79160cb5d25f4638996dc6330fad5860 |
|---|
| Source note | uspto-grants-2013_10 |
|---|