Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467282Generated: November 1, 2026

Pyridine → HCID 66746431, compound

https://huagongshe.com/reaction/1467282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 66745963HCID 66745963—
SolventDichloromethaneHCID 6344—
ProductHCID 66746431HCID 66746431100%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(8-hydroxyoctyloxy)-6-nitrobenzonitrile (804 μmol, 235 mg) (Example 214c) was dissolved in dry DCM (10 mL), cooled to 0° C., and treated successively with pyridine (3.216 mmol, 260 μL) and acetyl chloride (1.608 mmol, 114 μL). The reaction mixture was stirred and allowed to warm slowly to room temperature. When the reaction was complete, the volatiles were removed in vacuo and the crude product purified on silica gel (10% to 50% EtOAc in hexanes) to give the desired product (268 mg, 100%). MS 335 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000054B2
Source datasetuspto-grants-2015_04
ORD IDord-bb63e125b17c473d8c61980bd43ee5ec
Source noteuspto-grants-2015_04