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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347669Generated: October 27, 2026

Boron tribromide → 3'-Hydroxy-[1,1'-biphenyl]-3-carboxamide

https://huagongshe.com/reaction/347669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant3'-Methoxybiphenyl-3-carboxylic acid amideHCID 67122716—
SolventDichloromethaneHCID 6344—
Product3'-Hydroxy-[1,1'-biphenyl]-3-carboxamideHCID 5321855691%

Reaction Steps

To a stirred, cooled (0° C.) solution of 3′-methoxybiphenyl-3-carboxylic acid amide (0.57 g; 2.5 mmol) in dry CH2Cl2 (28 mL), under N2 atmosphere, a 1M solution of BBr3 in CH2Cl2 (6.4 mL) was added. The mixture was stirred at room temperature for 1 h, quenched with 2N Na2CO3 and extracted with AcOEt. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated. Purification of residue by column chromatography (cyclohexane/EtOAc 2:8) gave the desired product as an amorphous solid. Yield 91%. Mp: 148–51° C. (after digestion with i-Pr2O). MS (EI): m/z 213 (M+, 100%). 1H NMR (CDCl3/d6-DMSO): δ 6.06 (br s, 1H); 6.59 (m, 1H); 6.85 (m, 2H); 7.01 (t, 1H); 7.23 (t, 1H); 7.35 (br s, 1H); 7.45 (m, 1H); 7.60 (m, 1H) 7.88 (s, 1H); 8.80 (s, 1H) ppm. IR (Nujol): 3314, 3141, 1669, 1630, 1607, 1577 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176201B2
Source datasetuspto-grants-2007_02
ORD IDord-366361966fae45c79173a1ff7ec740af
Source noteuspto-grants-2007_02