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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297790Generated: October 30, 2026

Hydrochloric Acid → HCID 10127732, compound

https://huagongshe.com/reaction/1297790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant3-Tolylboronic acidHCID 2733950—
ReactantHCID 58914719HCID 58914719—
CatalystCupric acetateHCID 8895—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 10127732HCID 1012773234%

Reaction Steps

Combine 3,3-Bis-[4-(tert-butyl-dimethyl-silanyloxy)-3,5-dimethyl-phenyl]-1,3-dihydro-indol-2-one (0.650 g, 1.08 mmol), m-tolylboronic acid (0.294 g, 2.16 mmol), copper (II) acetate (0.196 g, 1.08 mmol), triethylamine (0.301 mL, 2.16 mmol), 4 angstrom molecular sieves, and dichloromethane (15 mL). Stir at room temperature overnight under ambient atmosphere. Filter the reaction through Celite. Elute through a column of silica gel with 70% dichloromethane in hexanes and concentrate. Dissolve the resulting compound (0.298 g, 0.431 mmol), in THF (4 mL). Add a solution of tetrabutylammonium fluoride (1.0 M) in THF (1.08 mL). Stir for 1 h. Add 1N aqueous HCl(10 mL),water (40 mL), and add ethyl acetate (50 mL). Separate the layers and concentrate the organic layer in vacuo. Chromatograph on silica gel eluting with ethyl acetate to give 0.170 g (34%) of the title compound: mass spectrum (FAB): m/z=413(M+1); 1H NMR(DMSO-d6): δ8.10 (s, 2H), 7.31 (t, 1H), 7.18-7.06 (m, 5H), 6.96 (t, 1H), 6.66-6.60 (m, 5H) 2.23 (s, 3H), 1.92 (s, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250442B2
Source datasetuspto-grants-2007_07
ORD IDord-311583bcc8204fe8861b1828c8be900b
Source noteuspto-grants-2007_07