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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601584Generated: October 30, 2026

Hydrochloric Acid → HCID 11581984, compound

https://huagongshe.com/reaction/601584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium BisulfiteHCID 23665763—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 66731247HCID 66731247—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11581984HCID 11581984—

Reaction Steps

Add a solution of oxone (0.18 g, 0.29 mmol) in water (2 mL) was added to a solution of 4-[4-(phenethylamino-methyl)-phenylsulfanyl]-benzamide (50 mg, 0.14 mmol), 1N aqueous hydrochloric acid (0.14 mL), and tetrahydrofuran (2 mL) at room temperature. Stir overnight at room temperature, pour into saturated aqueous sodium bisulfite, and then extract with ethyl acetate (3×50 mL). The combined ethyl acetate extracts were washed with saturated aqueous s odium bicarbonate solution, water, and brine then dried over sodium chloride/magnesium sulfate. Filter, and concentrate on a rotary evaporator to yield 100 mg of the crude product. The crude product is purified by flash column chromatography on silica gel eluting with (0.2% conc. ammonium hydroxide/2% ethanol) to (2% conc. ammonium hydroxide/20% ethanol) in chloroform to yield 4-[4-(Phenethylamino-methyl)-benzenesulfonyl]-benzamide, (15 mg): 1H NMR (DMSO-D6, 300.00 MHz): 9.06-9.01 (m, 1H), 8.50 (dd, 1H, J=8.1, 2.1 Hz), 8.31 (dd, 2H, J=8.2, 0.7 Hz), 7.96-7.81 (m, 3H), 7.61 (d, 2H, J=8.2 Hz), 7.32-7.15 (m, 6H), 3.88-3.82 (m, 2H), 2.78-2.71 (m, 4H); m/z=396.03 (M+1); HPLC=90% (5.81 minutes (5/95 to 95/5 ACN/(0.1% TFA in water) over 10 minutes, Zorbax SB-Phenyl 4.6 mm×15 cm×5 micron, λ=254 nM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902372B2
Source datasetuspto-grants-2011_03
ORD IDord-fc22ef5523a84082abbe8c1409cd5e81
Source noteuspto-grants-2011_03