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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038952Generated: October 31, 2026

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

https://huagongshe.com/reaction/2038952

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 numberUS08575118B2
Source datasetuspto-grants-2013_11
ORD IDord-2e4f38ca02de4e64b60940dbb0dfcec9
Source noteuspto-grants-2013_11