Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-chloropyridineHCID 817098—
ReactantHCID 178525802HCID 178525802—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58580279HCID 5858027963%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563583B2
Source datasetuspto-grants-2013_10
ORD IDord-79160cb5d25f4638996dc6330fad5860
Source noteuspto-grants-2013_10