Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852665Generated: October 31, 2026

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

https://huagongshe.com/reaction/1852665

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 numberUS08962607B2
Source datasetuspto-grants-2015_02
ORD IDord-d22b5e99bd984544a9b24866afb700e3
Source noteuspto-grants-2015_02