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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243561Generated: October 26, 2026

4-(Trimethylsilyl)phenylboronic Acid (contains varying amounts of Anhydride) → 1-(4-Trimethylsilanyl-phenyl)-isoquinoline

https://huagongshe.com/reaction/2243561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trimethylsilyl)phenylboronic Acid (contains varying amounts of Anhydride)HCID 1710—
ReactantCesium carbonateHCID 10796—
ReactantIsoquinoline, 1-chloro-HCID 140539—
ReactantDi-tert-butyl-trimethylsilylmethyl-phosphaneHCID 12583313—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-Trimethylsilanyl-phenyl)-isoquinolineHCID 25259833—

Reaction Steps

15.0 g (0.07727 mol) of 4-trimethylsilyl-phenylboronic acid, 10.11 g (0.0618 mol) 1-chloro-isoquinoline, 15.11 g (0.0464 mol) of cesium carbonate, 0.71 g (0.000775 mol) of tris(dibenzylideneacetone) dipalladium (0), 0.43 g (0.00185 mol) of di-tert-butyl-trimethylsilylmethyl-phosphane and 100 ml of dioxane were stirred at room temperature for 12 hr. The reaction mixture was filtered and the solvent was removed under vacuum. The resulting mixture was purified by chromatography on silica gel using petroleum ether/ethyl ether (10/0.5) as eluent. Yield of 1-(4-trimethylsilanyl-phenyl)-isoquinoline was 10.63 g (62%) as a colorless solid with m.p. 93.45° C. 1H NMR (CDCl3) 0.30 (s, 9H, Me3Si), 7.45-7.70 (m, 7H, arom-H), 7.85 (s, 1H, arom-H), 8.15 (s, 1H, arom-H), 8.51 (s, 1H, arom-H). Anal. Found: C, 77.68; H, 6.95; N, 4.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07675228B2
Source datasetuspto-grants-2010_03
ORD IDord-c991dd3eefa34ea99951ca3cfafd0200
Source noteuspto-grants-2010_03