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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185631Generated: November 4, 2026

Sodium borohydride → 4,4'-Dibromo-2,2'-bis-hydroxymethyl-biphenyl

https://huagongshe.com/reaction/1185631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4,4'-Dibromobiphenyl-2,2'-dicarbaldehydeHCID 11326094—
SolventMeOH tetrahydrofuranHCID 21899815—
Product4,4'-Dibromo-2,2'-bis-hydroxymethyl-biphenylHCID 1137217587%

Reaction Conditions

Temperature25 °C

Reaction Steps

The solution of 2,7-dibromo-phenanthrene (3.8 g) in DCM/MeOH (120 ml/1 ml) was cooled to −78° C., and it became a suspension. Ozone was bubbled thorough for 20 minutes, and the mixture became blue. Oxygen was bubbled for 5 minutes and dimethyl sulfide (3 ml) was added. The mixture was warmed to 25° C. and stirred for 12 hours. Concentration and purification by flash column chromatography (hexanes/EtOAc) gave 4,4′-dibromo-biphenyl-2,2′-dicarbaldehyde (600 mg). To the solution of 4,4′-dibromo-biphenyl-2,2′-dicarbaldehyde (600 mg, 1.7 mmol) in THF/MeOH (10 ml/10 ml) at 0° C. was added sodium borohydride (320 mg, 8.2 mmol). The mixture was warmed to 25° C. and stirred for 12 hours. The mixture was quenched with water, and extracted with EtOAc. The organic phase was washed with water and brine, and was dried with sodium sulfate. Concentration gave (4,4′-dibromo-2′-hydroxymethyl-biphenyl-2-yl)-methanol (550 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669234B2
Source datasetuspto-grants-2014_03
ORD IDord-5b7f894d816f4ca1828684d5e0ea460d
Source noteuspto-grants-2014_03