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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36267Generated: October 26, 2026

Ethanol → [2'-(N-t-Butylsulfamoyl)-5'n-propylbiphenyl-4-yl]methanol

https://huagongshe.com/reaction/36267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromobenzyl alcoholHCID 70119—
Reactant(2-(N-(tert-Butyl)sulfamoyl)-5-propylphenyl)boronic acidHCID 19939476—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product[2'-(N-t-Butylsulfamoyl)-5'n-propylbiphenyl-4-yl]methanolHCID 19939403—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2.80 g (9.36 mmol) of 2-(N-t-butylsulfamoyl)-5-n-propylphenylboronic acid (from Step B) and 4-bromobenzyl alcohol (5.25 g, 3 equiv) in toluene (125 mL) was added 1.25N NaOH (32 mL), EtOH (86 mL) and tetrakis(triphenylphosphine)palladium(0) (325 mg, 3 mol %). The mixture was stirred at 100° C. under N2 for 3 hours. The reaction was concentrated and the residue was extracted with ethyl acetate. The organic solution was washed with 1N NaOH, H2O and brine. Next, the organic phase was dried over anhydrous MgSO4 and concentrated in vacuo. The product was purified by flash chromatography, eluting with 2:1 hexane-EtOAc, to provide the titled compound; Rf =0.42 (1:1 EtOAc-hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411980
Source datasetuspto-grants-1995_05
ORD IDord-347e6008157e4bbaadb2cda22ee0054c
Source noteuspto-grants-1995_05