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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095273Generated: October 31, 2026

Hydrochloric Acid → HCID 68938521, compound

https://huagongshe.com/reaction/2095273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCesium fluorideHCID 25953—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant2-Methylphenyl boronic acidHCID 2733267—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
ReactantHCID 68936013HCID 68936013—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68938521HCID 68938521—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of EXAMPLE 402D (47 mg), o-tolylboronic acid (19 mg), tris(dibenzylidineacetone)dipalladium(0) (4.6 mg), tri-t-butyl-phosphonium tetrafluoroborate (3.5 mg), cesium fluoride (45.6 mg) and tetrahydrofuran (1.5 ml) was stirred at ambient temperature under a nitrogen atmosphere overnight. Additional o-tolylboronic acid (9.5 mg), tris(dibenzylidineacetone)dipalladium(0) (2.3 mg), tri-t-butyl-phosphonium tetrafluoroborate (1.8 mg) and cesium fluoride (23 mg) were added and stirring was continued at ambient temperature overnight. LiOH—H2O (42 mg) and water (0.5 ml) were added and the mixture was heated overnight at 60° C. The reaction mixture was acidified with 1 M HCl (aq), extracted (3×5 ml) with ethyl acetate, dried (MgSO4), filtered and concentrated. The concentrate was slurried in methanol and filtered through a syringe filter. The filtrate was concentrated. The concentrate was purified by reverse phase HPLC (50-95% acetonitrile/water/0.1% trifluoroacetic acid). 1H NMR (300 MHz, DMSO-d6) □ 13.10 (s, 1H), 10.86 (s, 1H), 8.20 (m, 1H), 7.86 (m, 1H), 7.48 (m, 4H), 7.28 (m, 4H), 6.99 (m, 1H), 6.90 (m, 2H), 4.23 (t, 2H), 3.45 (t, 2H), 2.25 (m, 2H), 2.05 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445679B2
Source datasetuspto-grants-2013_05
ORD IDord-581e241377c24545ae504674323a676d
Source noteuspto-grants-2013_05