Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013146Generated: October 25, 2026

Water → (6-Methyl-[1,1'-biphenyl]-3-yl)methanol

https://huagongshe.com/reaction/1013146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant3-Iodo-4-methylbenzyl alcoholHCID 5166798—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
Solvent1-PropanolHCID 1031—
Product(6-Methyl-[1,1'-biphenyl]-3-yl)methanolHCID 2308911388.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of compound PPP, (3-iodo-4-methyl-phenyl)-methanol, (4 g, 16.12 mmol) and phenylboronic acid (2.06 g, 16.89 mmol) in 1-propanol (30 mL) was successively added palladium(II) acetate (0.01276 g, 0.05 mmol), triphenyl phosphine (0.042 g, 0.161 mmol), aq. sodium carbonate solution (2 M, 11.44 mL, 22.88 mmol), and water (6 mL). The mixture was heated to 100° C. until reaction is complete (tlc), cooled, quenched with water (20 mL) and extracted into ethyl acetate (3×50 mL). Combined organic layer was washed with 2% aq. sodium bicarbonate (2×25 mL), brine (1×50 mL), dried (MgSO4) and concentrated to yield 2.82 g of (6-methyl-biphenyl-3-yl)-methanol, compound QQQ, that was directly taken into next step without any further purification; Rt: 10.95 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981907B2
Source datasetuspto-grants-2011_07
ORD IDord-462e16135bfd4fd4924ff1c197cd328f
Source noteuspto-grants-2011_07