Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910140Generated: October 30, 2026

Hydrochloric Acid → HCID 57743111, compound

https://huagongshe.com/reaction/910140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant3-Thiophenacetic acidHCID 23404—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Bromo-1-(4-chlorophenyl)propan-1-oneHCID 3788219—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 57743111HCID 57743111—

Reaction Steps

To a mixture of 3.08 g of 2-bromo-4′-chloropropiophenone, 1.79 g of 3-thiopheneacetic acid, acetonitrile and 10 ml of DMF was added 1.53 g of triethylamine, and the mixture was stirred for 2 hours at room temperature. The resultant mixture was cooled to 0° C., and 4.60 g of 1,8-diazabicyclo[5.4.0]undec-7-ene was added dropwise into this, and the mixture was stirred for 3 hours at room temperature. Then, the reaction mixture was stirred for 11 hours at room temperature while blowing air into the reaction mixture. To the reaction mixture was added 200 ml of 1 mol/L hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and saturated brine sequentially, and dried over anhydrous magnesium sulfate, then, concentrated under reduced pressure to obtain 3.98 g of 4-(4-chlorophenyl)-5-hydroxy-5-methyl-3-(3-thienyl)-2(5H)-furanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022073B2
Source datasetuspto-grants-2011_09
ORD IDord-451bb585a6304c83a094bf0a22adb07f
Source noteuspto-grants-2011_09