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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578791Generated: October 31, 2026

Water → HCID 68993601, compound

https://huagongshe.com/reaction/578791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 24721179HCID 24721179—
SolventDimethylformamideHCID 6228—
ProductHCID 68993601HCID 68993601—

Reaction Steps

To a solution of 4-chloro-3-nitrothiophenol (0.4 g) and benzyl bromide (0.3 mL) in N,N-dimethylformamide (6 mL) was added potassium carbonate (0.44 g), and the mixture was stirred at room temperature for 15 minutes. To the reaction mixture was added water, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and brine successively, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane −n-hexane/ethyl acetate=9/1) to give 1-benzylthio-4-chloro -3-nitrobenzene (0.54 g). This material was dissolved in methanol (5 mL)-tetrahydrofuran (5 mL). To the solution were added nickel (II) bromide (21 mg) and sodium borohydride (0.22 g) under ice-cooling, and the mixture was stirred at the same temperature for 30 minutes. The mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with ethyl acetate, and the resulting mixture was washed with a saturated aqueous sodium hydrogen carbonate solution, water and brine successively, and dried over anhydrous magnesium sulfate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040693B2
Source datasetuspto-grants-2015_05
ORD IDord-9c64acdc0a494450b32fa21326d9eec0
Source noteuspto-grants-2015_05