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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043436Generated: October 31, 2026

4'-Bromo-4-(dimethylamino)biphenyl-2-carboxylic acid → (4'-Bromo-4-(dimethylamino)biphenyl-2-yl)methanol

https://huagongshe.com/reaction/1043436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-Bromo-4-(dimethylamino)biphenyl-2-carboxylic acidHCID 59266564—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(4'-Bromo-4-(dimethylamino)biphenyl-2-yl)methanolHCID 5926657498%

Reaction Steps

4′-bromo-4-(dimethylamino)biphenyl-2-carboxylic acid (1.34 g, 4.19 mmol) in THF (40 mL) was cooled to 0° C. Borane tetrahydrofuran complex (8.37 mL, 8.37 mmol) was added dropwise over 15 min. and allowed to warm up to r.t. overnight. The reaction was diluted with EtOAc and washed with water, saturated ammonium chloride, and then brine. The organic layer was dried over MgSO4, filtered and evaporated to give (4′-bromo-4-(dimethylamino)biphenyl-2-yl)methanol (1.25 g, 4.08 mmol, 98% yield) as a white solid. 1H NMR (500 MHz, CHLOROFORM-d) δ ppm 2.93-3.05 (m, 6H) 4.58 (s, 2H) 6.72 (dd, J=8.55, 2.75 Hz, 1H) 6.90 (d, J=2.75 Hz, 1H) 7.14 (d, J=8.55 Hz, 1H) 7.21-7.25 (m, 2H) 7.44-7.55 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563505B2
Source datasetuspto-grants-2013_10
ORD IDord-335509e11a5a4b3da569bd77234f2f19
Source noteuspto-grants-2013_10