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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365919Generated: November 3, 2026

Benzyl Alcohol → HCID 70921751, compound

https://huagongshe.com/reaction/2365919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant1,2,4-Trifluoro-5-nitrobenzeneHCID 75012—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70921751HCID 70921751—

Reaction Steps

2.82 g (70.6 mmol, 2.5 eq) of sodium hydride at 60% are added to a solution of 7.6 g (70.6 mmol, 2.5 eq) of benzyl alcohol in 100 ml of tetrahydrofuran. The reaction medium is stirred at ambient temperature for 1½ hours and then 5.0 g (28.2 mmol, 1 eq) of 1,2,4-trifluoro-5-nitrobenzene in solution in 50 ml of tetrahydrofuran are added dropwise. The reaction medium is refluxed for 3 hours. The reaction medium is treated with 150 ml of 1M hydrochloric acid and extracted with ethyl acetate. The organic phases are combined, washed with a saturated solution of sodium chloride, dried over magnesium sulphate, filtered and evaporated. The residue is chromatographed on silica gel, elution being carried out with 90/10 heptane/ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697726B2
Source datasetuspto-grants-2014_04
ORD IDord-b11220fafd604b099d047444dbb673c5
Source noteuspto-grants-2014_04