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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23864Generated: October 29, 2026

Phenylboronic Acid → (2-Phenyl-3,4,5-trimethoxyphenyl)diphenylphosphine oxide

https://huagongshe.com/reaction/23864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
Reactant(2-Iodo-3,4,5-trimethoxyphenyl)diphenylphosphine oxideHCID 14906789—
CatalystHCID 178418397HCID 178418397—
Product(2-Phenyl-3,4,5-trimethoxyphenyl)diphenylphosphine oxideHCID 1299624598%

Reaction Steps

To a 2 liter Schlenk flask was added (2-iodo-3,4,5-trimethoxyphenyl) diphenylphosphine oxide 21 (30 g, 61 mmol), phenylboronic acid (11.1 g, 91 mmol), and degassed THF (800 ml). A solution of degassed saturated K2CO3 (400 ml) was added afterwards. The whole mixture was degassed with nitrogen for an additional 10 min. Then, Pd(PPh3)4 (1.22 mmol, 1.4 g) was added in the solution through one portion. The mixture was stirred at reflux under nitrogen for 24 hrs. In situ 31PNMR showed that the reaction was complete. The reaction mixture was concentrated under reduced pressure to remove THF and 400 ml of CH2Cl2 was then added. The CH2Cl2 layer was washed with water (200 ml) and brine (200 ml), dried over Na2SO4, and evaporated. The solid residue was recrystallized from EtOAc (100 ml) to give off-white product 22 (23 g). The mother liquid was passed though a silica gel column to give another 4 g of product 22. The total yield was 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855657B2
Source datasetuspto-grants-2005_02
ORD IDord-d0ee01d0729c4903be151f6d627b25e5
Source noteuspto-grants-2005_02