Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021333Generated: October 31, 2026

4-Chlororesorcinol → HCID 67166662, compound

https://huagongshe.com/reaction/1021333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlororesorcinolHCID 1731—
Reactant3-Chloropropionic acidHCID 7899—
ReactantTrifluoromethanesulfonic acidHCID 62406—
SolventWaterHCID 962—
ProductHCID 67166662HCID 6716666298.6%

Reaction Conditions

Temperature6 °C

Reaction Steps

A 2-liter 4-neck round-bottom flask was charged with trifluoromethanesulfonic acid (500 g, 3.33 mol) and the flask contents were cooled below 10° C. 4-Chlororesorcinol (100 g, 0.69 mol) was added in portions over 20-30 minutes, maintaining the temperature at 4 to 8° C. The reaction mixture was stirred at or below 10° C. until a clear solution formed (40 minutes). 3-Chloropropanoic acid (78.8 g, 0.73 mol) was warmed until melted and then added in liquid form dropwise over 45 minutes to the flask, maintaining the temperature at or below 10° C. The reaction mixture was stirred for an additional 10 minutes at or below 10° C., then slowly heated to 50-55° C. and maintained there for 6 hours. The reaction mixture was cooled to ambient temperature and added dropwise to water (1.1 L) contained in a 3-liter 4-neck round-bottom flask. The resulting mixture was stirred at ambient temperature for 30 minutes. The resulting precipitate was collected by filtration, washed with water (3×540 mL), and dried in a fan dryer at 40° C. until the moisture content fell below 0.5%, to afford 3-chloro-1-(5-chloro-2,4-dihydroxyphenyl)propan-1-one as an orange solid (160 g, 98.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716498B2
Source datasetuspto-grants-2014_05
ORD IDord-cb65112768fe4931a99f6c2086b8985a
Source noteuspto-grants-2014_05