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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362126Generated: November 2, 2026

Potassium Phosphate, Tribasic → 1-tert-Butyl 6-methyl 3-phenyl-1H-indole-1,6-dicarboxylate

https://huagongshe.com/reaction/2362126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
Reactant1-tert-butyl 6-methyl 3-iodo-1H-indole-1,6-dicarboxylateHCID 7127827—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product1-tert-Butyl 6-methyl 3-phenyl-1H-indole-1,6-dicarboxylateHCID 59626044—

Reaction Steps

A mixture of 1-tert-butyl 6-methyl 3-iodo-1H-indole-1,6-dicarboxylate 62a (5.02 mmol, 2.016 g), phenylboronic acid 1x (7.53 mmol, 0.92 g), Pd(OAc)2 (0.402 mmol, 90 mg), Sphos 0.904 mmol, (0.37 g), and K3PO4 (10.1 mmol, 2.13 g) in toluene (10 mL) in sealed reaction vial was stirred at room temperature for 2 min and then heated at 90° C. under N2 for 4 h. The reaction mixture was quenched with EtOAc and water. The organic layer was concentrated and purified by flash column chromatography (silica gel, 8% EtOAc/hexanes). The desired product was collected as a light yellow solid that was washed with small amount of hexanes to obtain 62b as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691805B2
Source datasetuspto-grants-2014_04
ORD IDord-fd22ff54163c4dfa9c9e6f223dc04e8d
Source noteuspto-grants-2014_04