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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662376Generated: October 29, 2026

Potassium Phosphate, Tribasic → Methyl 4-(benzyloxy)-3-(5,5-dimethylcyclopent-1-enyl)benzoate

https://huagongshe.com/reaction/1662376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantMethyl 4-(benzyloxy)-3-bromobenzoateHCID 23111814—
Reactant2-(5,5-Dimethylcyclopent-1-enyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 57467587—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-(benzyloxy)-3-(5,5-dimethylcyclopent-1-enyl)benzoateHCID 57467616386.5%

Reaction Conditions

Temperature75 °C

Reaction Steps

A stirred mixture of 66.11C (3.75 g, 11.66 mmol), ground S-Phos (0.96 g, 2.33 mmol), palladium acetate (0.26 g, 1.17 mmol), and potassium phosphate, tribasic (6.19 g, 29.17 mmol) in DMF (28.0 mL) and water (1.50 mL) was purged three times with argon and placed under vacuum three times. Before heating, 2-(5,5-dimethylcyclopent-1-enyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (66.6C) (3.11 g, 13.99 mmol) was added via syringe, then the mixture was heated to 75° C. After 21 hours (black solution), the reaction was cooled to room temperature, diluted with water, and extracted three times with EtOAc. The combined organic layers were washed twice with brine. After drying over anhydrous sodium sulfate and filtration, the organic solvent was removed under reduced pressure. The residue was purified on silica gel (0-10% EtOAc in hexanes) to yield 66.11D as a colorless oil (3.03 g, 77%). MS ESI (pos.) m/e: 337.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-09699f87ae7843cb93df41bc2d197b8d
Source noteuspto-grants-2011_10