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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921591Generated: October 25, 2026

Methanol → 3-Bromopropiophenone thiosemicarbazone

https://huagongshe.com/reaction/1921591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-Bromo-1-phenylpropan-1-oneHCID 122432—
ReactantThiosemicarbazideHCID 2723789—
SolventAcetic AcidHCID 176—
Product3-Bromopropiophenone thiosemicarbazoneHCID 8662882742.8%

Reaction Steps

(Du, X.; Guo, C.; Hansell, E.; Doyle, P. S.; Caffrey, C. R.; Holler, T. P.; McKerrow, J. H.; Cohen, F. E. J. Med. Chem. 2002, 45, 2695-2707) Into a round bottom flask containing 3-bromopropiophenone (0.508 g, 2.34 mmol), 20 mL of anhydrous methanol were added and the solution was refluxed for 15 minutes. To the warm ketone solution, thiosemicarbazide (0.184 g, 2.04 mmol) and 1% solution of HOAc (0.2 mL) were added. The reaction mixture was refluxed under nitrogen atmosphere for 17 h, at which point, the solvent was evaporated and, the crude reaction mixture was purified by flash chromatography (30% EtOAc/70% hex) to obtain 0.2498 g (0.873 mmol) of the product in a 37% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173696B2
Source datasetuspto-grants-2012_05
ORD IDord-fc12a2f8699b427d95bd82c55176c585
Source noteuspto-grants-2012_05