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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371155Generated: October 31, 2026

Pyridine → HCID 57656651, compound

https://huagongshe.com/reaction/2371155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
Reactant3-BenzyloxyanilineHCID 92892—
SolventDichloromethaneHCID 6344—
ProductHCID 57656651HCID 57656651—

Reaction Steps

To a stirred solution of 3-benzyloxyaniline (0.999 g, 5.01 mmol) in DCM (10 mL) was added pyridine (1.22 ml, 15.03 mmol) and phenyl chloroformate (0.68 ml, 5.51 mmol) dropwise (Exotherm!). The reaction was then allowed to stir at room temperature for 2 hours. The reaction mixture was then partitioned between DCM and 1M HCl, extracted twice, combined organics passed through phase separating cartridge and filtrate evaporated to dryness to give an orange solid. This was then triturated in 10% ethyl acetate/hexanes, filtered and dried to give the product, phenyl [3-(benzyloxy)phenyl]carbamate, as beige solid (1.209 g, 3.78 mmol, 75% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710224B2
Source datasetuspto-grants-2014_04
ORD IDord-9bd63c0b6b9a447086810ad188b38dc1
Source noteuspto-grants-2014_04