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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69950Generated: October 26, 2026

Pyridine → Benzyl (4-chloropyridin-3-yl)carbamate

https://huagongshe.com/reaction/69950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzyl chloroformateHCID 10387—
Reactant3-Amino-4-chloropyridineHCID 581932—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl (4-chloropyridin-3-yl)carbamateHCID 6904293334%

Reaction Steps

A solution of benzyl chloroformate (1.1 equiv.) in THF (1.85 M) was slowly added to a solution of 3-amino-4-chloropyridine (1.0 equiv.) and pyridine (1.5 equiv.) in THF (1.0 M) and stirred at rt for 3.5 hours (formation of a precipitate over time). The reaction was quenched with H2O (100 mL), extracted with EtOAc (200 mL), washed with NaCl(sat.) (75 mL), dried over MgSO4, filtered and the volatiles were removed in vacuo. The product precipitated from a mixture of hexane/EtOAc yielding benzyl 4-chloropyridin-3-ylcarbamate (34%). LCMS (m/z): 263.1 (MH+); LC Rt=2.33 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822497B2
Source datasetuspto-grants-2014_09
ORD IDord-fe4cb553cd4346b4a655937987b025fe
Source noteuspto-grants-2014_09