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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538861Generated: October 31, 2026

Potassium Phosphate, Tribasic → 4-(4-tert-Butylphenyl)-6-(cyclohexylmethyl)-1,2,3,5-tetrahydro-s-indacene

https://huagongshe.com/reaction/538861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-tert-Butylphenylboronic acidHCID 2734320—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant4-Bromo-6-(cyclohexylmethyl)-1,2,3,5-tetrahydro-s-indaceneHCID 66615608—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-(4-tert-Butylphenyl)-6-(cyclohexylmethyl)-1,2,3,5-tetrahydro-s-indaceneHCID 86693797—

Reaction Conditions

Temperature100 °C

Reaction Steps

In argon atmosphere, a mixture of 34.6 g (105 mmol) of 4-bromo-6-(cyclohexylmethyl)-1,2,3,5-tetrahydro-s-indacene, 22.4 g (126 mmol) 4-tert-butylphenylboronic acid, 66.8 g (315 mmol) of K3PO4, 1.21 g (21 mmol) of Pd(dba)2, 1.73 g (42 mmol) of dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine and 350 ml of toluene was stirred for 12 h at 100° C. The resulting mixture was cooled to room temperature, and then 600 ml of water was added. The organic layer was separated, and the aqueous layer was extracted with 3×100 ml of dichloromethane. The combined organic extract was dried over Na2SO4 and then evaporated to dryness. The target product was isolated by flash chromatography on silica gel 60 (40-63 um; eluent: hexanes). Yield 24.0 g (62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865848B2
Source datasetuspto-grants-2014_10
ORD IDord-d84dcb5bdd884e9fa3aabd107a14a6e5
Source noteuspto-grants-2014_10