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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815475Generated: October 31, 2026

2-Chlorobenzaldehyde → HCID 9890542, compound

https://huagongshe.com/reaction/1815475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant2-ThiocresolHCID 8712—
Reactant6-Amino-1-hexanolHCID 19960—
Reactant2,4-DichlorobenzenethiolHCID 70730—
Reactant1-(3-Aminopropyl)-2-pyrrolidinoneHCID 82111—
Reactant4-Fluoro-3-(trifluoromethyl)benzaldehydeHCID 522269—
ProductHCID 9890542HCID 9890542—

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 3-(2-oxopyrrolidin-1-yl)propylamine. 1H NMR (CDCl3, 300 MHz) δ 7.78 (s, 1H); 7.53 (d, J=15.6 Hz, 1H); 7.49 (d, J=7.2 Hz, 1H); 7.40-7.33 (m, 3H); 7.14 (m, 1H); 6.80 (d, J=8.2 Hz, 1H); 6.43 (d, J=15.6 Hz, 1H); 3.41 (m, 4H); 3.32 (q, J=6.1 Hz, 2H); 2.43 (t, J=6.6 Hz, 2H); 2.34 (s, 3H), 2.08 (m, 2H), 1.75 (m, 2H). MS (ESI) m/z 947 (2M+Na)+, 925 (2M+H)+, 485 (M+Na)+, 463 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878700B1
Source datasetuspto-grants-2005_04
ORD IDord-af932ab7b8a54483a5eb54c930222ad5
Source noteuspto-grants-2005_04