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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661448Generated: November 2, 2026

Hydrochloric Acid → HCID 57972811, compound

https://huagongshe.com/reaction/661448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
Reactant(3R)-3-Aminopentanoic acid hydrochlorideHCID 66557334—
CatalystCopper iodideHCID 83717—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 57972811HCID 57972811—

Reaction Conditions

Temperature110 °C

Reaction Steps

To (R)-3-aminovaleric acid hydrochloride (5.0 g), were added 1-bromo-4-trifluoromethylbenzene (10.95 g), copper iodide (1.24 g), potassium carbonate (13.5 g) and dimethylsulfoxide (50 ml), the mixture was stirred under nitrogen atmosphere in a sealed vessel at about 110° C. for 46 hours. The reaction mixture was cooled, water (50 ml) and toluene (50 ml) was added thereto, the pH was adjusted to 3-4 with addition of hydrochloric acid (12.5 mL) and the solution was separated. The aqueous layer was extracted with toluene (50 ml) and the combined organic layer was washed with water (50 ml). 28% ammonia water (50 ml) and water (50 ml) were added to the organic layer and the product was extracted with the aqueous layer. To the aqueous layer were added toluene (50 ml) and hydrochloric acid (30 ml) and the solution was separated. The organic layer was concentrated in vacuo at about 60° C. of the bath temperature, n-heptane (16.3 g) was added to the residue and evaporated twice to give the titled compound as an oily residue. The product was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084611B2
Source datasetuspto-grants-2011_12
ORD IDord-ae3f904c5c4c4566895ac4116f6eea51
Source noteuspto-grants-2011_12