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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815473Generated: October 30, 2026

2-Chlorobenzaldehyde → HCID 9846498, compound

https://huagongshe.com/reaction/1815473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant2-ThiocresolHCID 8712—
Reactant6-Amino-1-hexanolHCID 19960—
Reactant2,4-DichlorobenzenethiolHCID 70730—
Reactant1-AcetylpiperazineHCID 83795—
Reactant4-Fluoro-3-(trifluoromethyl)benzaldehydeHCID 522269—
ProductHCID 9846498HCID 9846498—

Reaction Steps

The title compound was prepared by the procedures described in Example 1 substituting 2,4-dichlorothiophenol with 2-methylthiophenol, 2-chlorobenzaldehyde with 4-fluoro-3-trifluoromethyl benzaldehyde, and 6-amino-1-hexanol with 1-acetylpiperazine. 1H NMR (CDCl3, 300 MHz) δ 7.79 (s, 1H); 7.63 (d, J=15.4 Hz, 1H); 7.51 (d, J=6.8 Hz, 1H); 7.41-7.33 (m, 3H); 7.28 (m, 1H); 6.83 (d, J=15.4 Hz, 1H); 6.79 (d, J=6.8 Hz, 1H); 3.80-3.60 (m, 6H); 3.57-3.50 (m, 2H); 2.34 (s, 3H); 2.14 (s, 3H). MS (ESI) m/z 919 (2M+Na)+, 897 (2M+H)+, 471 (M+Na)+, 449 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878700B1
Source datasetuspto-grants-2005_04
ORD IDord-b3d89af261eb482a92bd2f41d50e6b60
Source noteuspto-grants-2005_04