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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11892Generated: October 29, 2026

Sodium borohydride → HCID 68562257, compound

https://huagongshe.com/reaction/11892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3,5-Dibromo4-(n,n-dimethylsulfamoyl)benzaldehydeHCID 21976884—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68562257HCID 6856225798.3%

Reaction Steps

To a solution of OBS02013 (5.5 g, 14.21 mmol) in anhydrous THF (50 mL) was added sodium borohydride (0.59 g, 15.63 mmol). The mixture was stirred at room temperature for 4 h, quenched with water (CARE!!) and filtered through a Celite pad. The filtrate was concentrated in vacuo and re-dissolved in DCM (200 mL). The organic layer was washed with brine (2×200 mL), dried (Na2SO4) and filtered. Concentration in vacuo of the combined filtrates gave OBS02015 as a pale yellow oil (5.21 g, 94%). TLC [SiO2, EtOAc-n-hexane (1:1)] Rf=0.55; 1H-NMR (270 MHz, CDCl3)=1.97 (1H, bs, OH), 3.11 (6H, s), 4.63 (2H, s), 7.55 (2H, t, J=1.5). 3,5-Dibromo-4-(N,N-dimethylsulfamoyl)benzyl chloride (OBS02018)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098343B2
Source datasetuspto-grants-2006_08
ORD IDord-bed968cd268c4dc9bd3f8edd0f8cf451
Source noteuspto-grants-2006_08