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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182816Generated: October 31, 2026

4-Chlorobenzoyl chloride → HCID 10193724, compound

https://huagongshe.com/reaction/2182816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantHCID 22481057HCID 22481057—
ProductHCID 10193724HCID 10193724—

Reaction Steps

Following the protocol of Example 8 and employing (6-chloropyridin-3-yl)-(1-methyl-1H-pyrrol-2-yl)methanone hydrochloride in place of (1-methyl-1H-pyrrol-2-yl)-pyridin-3-ylmethanone hydrochloride and 4-chlorobenzoyl chloride in place of 4-fluorobenzoyl chloride, the title compound was obtained and recrystallized from MTBE: mp 150-152° C. ES-MS m/z=360 (M++H). 1H NMR (300 MHz, CDCl3) δ 4.1 (s, 3H); 7.2 (s, 1H); 7.5 (m, 3H); 7.56 (s, 1H); 7.8 (dd, 2H); 8.05 (d, 1H); 8.8 (s, 1H). Anal calc'd for C18H12C2N2O2: 60.19; H, 3.37; N, 7.8. Found: C, 59.9; H, 3.34; N, 7.71.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897319B2
Source datasetuspto-grants-2005_05
ORD IDord-31792df5bb3e4017aa0b57610cc7be7a
Source noteuspto-grants-2005_05