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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984320Generated: October 31, 2026

Sodium Carbonate → 3-(5'-Isopropyl-2'-methoxy-biphenyl-4-yl)-but-2-en-1-ol

https://huagongshe.com/reaction/984320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Isopropyl-2-methoxyphenylboronic acidHCID 4589190—
Reactant(E)-3-(4-bromophenyl)but-2-en-1-olHCID 69361278—
SolventHydrochloric AcidHCID 313—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-(5'-Isopropyl-2'-methoxy-biphenyl-4-yl)-but-2-en-1-olHCID 69796935—

Reaction Steps

Tetrakis(triphenylphoshine)palladium(0) (0.20 g, 0.18 mmol, 4 mol %) was added, under nitrogen, to a stirred solution of (E)-3-(4-bromophenyl)-but-2-en-1-ol (1.0 g, 4.40 mmol) {prepared as detailed in example 50 b} in DME (55 ml), and the resulting orange coloured solution stirred at room temperature for 10 min. Aqueous 2M sodium carbonate (13.2 ml, 26.4 mmol) was then added, the mixture stirred for 10 min, then 5-isopropyl-2-methoxyphenylboronic acid (1.28 g, 6.60 mmol) was added, and the reaction mixture heated to 80° C. for 18 h, under reflux. The reaction mixture was diluted with 1N HCl (100 ml) and the products extracted into ethyl acetate (2×100 ml). The combined organic extracts were washed with brine, dried (MgSO4), and evaporated to give the crude product, which was purified by column chromatography on silica gel (1% methanol in dichloromethane eluent) to give the product, 3-(5′-isopropyl-2′-methoxy-biphenyl-4-yl)-but-2-en-1-ol as a colourless oil; 1.15 g (88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867218B2
Source datasetuspto-grants-2005_03
ORD IDord-45b7ae7383fa4f2ab864200890004167
Source noteuspto-grants-2005_03