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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235443Generated: October 31, 2026

Pyridine → HCID 23092680, compound

https://huagongshe.com/reaction/2235443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroformHCID 6212—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantHCID 22162178HCID 22162178—
SolventDichloromethaneHCID 6344—
ProductHCID 23092680HCID 23092680—

Reaction Steps

To a solution of C1 (3.1 g) and dry pyridine (3.5 ml; 42 mmol) in dry CH2Cl2 (75 ml) is added 4-methoxy-benzoyl chloride (2.63 g; 15.4 mmol) over a period of 2 min. After addition the mixture is stirred at RT for 20 h. CHCl3 (200 ml) is added and the organic layer is washed with sodium hydroxide solution (0.5 N) and water, dried over MgSO4 and concentrated in vacuo. The crude material is triturated with boiling EtOH and the precipitate is collected by filtration (3.73 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714010B2
Source datasetuspto-grants-2010_05
ORD IDord-d28c0b0577c44c73b5686cb6a54fe9e1
Source noteuspto-grants-2010_05