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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716849Generated: October 29, 2026

1,3-Dichloroacetone → HCID 57550208, compound

https://huagongshe.com/reaction/1716849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
ReactantHCID 24700409HCID 24700409—
SolventEthanolHCID 702—
ProductHCID 57550208HCID 5755020860%

Reaction Steps

A stirred solution of 4-(1H-benzimidazol-1-ylmethyl)benzenecarbo-thioamide (0.50 g, 1.87 mmol) in ethanol was treated with 1,3-dichloroacetone (0.235 g, 1.85 mmol), heated at reflux temperature for 3 h, allowed to cool to room temperature and filtered. The filtercake was washed with cold ethanol and dried under vacuum to afford the title compound in 60% yield, identified by NMR and mass spectral analyses. 1H NMR (400 MHz, CDCl3): 4.85 (s, 2H), 5.67 (s, 2H), 7.34-7.35 (m, 2H), 7.48 (d, J=7.6 Hz, 2H), 7.64-7.65 (m, 1H), 7.74-7.76 (m, 1H), 7.80 (s, 1H), 7.92 (d, J=7.6 Hz, 2H), 8.94 (s, 1H). LCMS (ESI+) 340 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803825B2
Source datasetuspto-grants-2010_09
ORD IDord-4416b17eab8d45e79452317a847504f7
Source noteuspto-grants-2010_09