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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402837Generated: October 30, 2026

3,5-Dichlorobenzylic alcohol → HCID 66764611, compound

https://huagongshe.com/reaction/402837

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichlorobenzylic alcoholHCID 43236—
Reactant2,6-Dichloro-4′-fluoro[1,1′-biphenyl]-4-carboxylic acidHCID 66764980—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66764611HCID 66764611—

Reaction Steps

To a solution of 2,6-dichloro-4′-fluorobiphenyl-4-carboxylic acid (350 mg, 1.155 mmol) in THF (5 mL) was added 2M borane-methyl sulfide complex in THF (0.35 mL, 0.70 mmol) at room temperature. After 20 hours, the reaction was quenched with 2M HCl and water and was extracted twice with ethyl acetate. The organic layers were washed with brine containing some aqueous sodium bicarbonate, dried over sodium sulfate, combined and concentrated. The residue was purified on silica gel (COMBI FLASH 12 gm column, 100% DCM, then a gradient of 2-10% ethyl acetate/DCM) to give a single main band by TLC (65 mg) containing a 1:1 mixture of title intermediate and 3,5-dichlorobenzyl alcohol from the Step 1 bi-product impurity. The mixture was used directly in Step 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742110B2
Source datasetuspto-grants-2014_06
ORD IDord-43b898746b374d3d9e1bf52a210b87fc
Source noteuspto-grants-2014_06