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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046802Generated: October 31, 2026

Hydrochloric Acid → HCID 59139149, compound

https://huagongshe.com/reaction/1046802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant18-Crown-6HCID 28557—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 59139173HCID 59139173—
SolventAcetonitrileHCID 6342—
ProductHCID 59139149HCID 5913914970.2%

Reaction Steps

Acetonitrile (1.0 mL) was added to dimethylcarbamic acid 4-bromomethyl-3-(2-fluoro-3-nitrobenzyl)-2-oxo-2H-1-benzopyran-7-yl ester (compound 6b-1-4) (24.0 mg), and potassium fluoride (3.1 mg) and 18-crown-6 (13.2 mg) were added to the resultant suspension while stirring at room temperature. The mixture was stirred at 60° C. for 4 hours, potassium fluoride (3.1 mg) and 18-crown-6 (13.2 mg) were then added to the reaction solution, and the mixture was further stirred at 60° C. for 1.5 hours. This reaction solution was poured into 1N hydrochloric acid (0.110 mL) diluted with ice water (20 mL), and then extracted with ethyl acetate. The resultant organic layer extraction liquid was washed with saturated saline, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure, and the resultant residue was purified by thin layer silica gel chromatography (hexane:ethyl acetate=1:1) to yield the title compound (14.7 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569378B2
Source datasetuspto-grants-2013_10
ORD IDord-a1a1634ed76946b296a46cffe47f92f1
Source noteuspto-grants-2013_10