Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989259Generated: October 29, 2026

Pyridine → HCID 12015902, compound

https://huagongshe.com/reaction/989259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 12015901HCID 12015901—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 12015902HCID 12015902—

Reaction Steps

To a solution of the compound obtained in Step B (6.2 g/0.03 mol) in 100 ml of CH2Cl2 there are added, in succession, pyridine (4.9 ml/0.06 mol), DMAP (1.83 g/0.015 mol), and then, dropwise, acetic anhydride (5.7 ml/0.06 mol). The whole is then stirred at room temperature for 24 hours. The reaction mixture is then concentrated to dryness, taken up in AcOEt, washed with a dilute HCl solution (1N), a saturated NaHCO3 solution and then with a saturated NaCl solution; dried over MgSO4 and then concentrated to dryness. The residual yellowish oil is then purified by chromatography over silica gel to yield the title product in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638962B2
Source datasetuspto-grants-2003_10
ORD IDord-bef01ffbfea742809dc3c1f5c79daa05
Source noteuspto-grants-2003_10