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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11890Generated: October 29, 2026

Sodium borohydride → 3-Bromo4-(N,N-dimethylsulfamoyl)benzyl alcohol

https://huagongshe.com/reaction/11890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Bromo-4-(N,N-dimethylsulfamoyl)benzaldehydeHCID 21976919—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo4-(N,N-dimethylsulfamoyl)benzyl alcoholHCID 6575101896.7%

Reaction Steps

To a solution of OBS02001 (6.0 g, 19.47 mmol) in anhydrous THF (50 mL) was added sodium borohydride (0.81 g, 21.42 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 filtrates gave OBS02002 as a pale yellow oil (5.54 g, 92%). TLC [SiO2, EtOAc-n-hexane (1:1)] Rf=0.47; 1H-NMR (270 MHz, CDCl3)=2.97 (6H, s), 3.14 (1H, bs, OH), 4.51 (2H, s), 7.19 (1H, dd, J=1.5, 8.1), 7.37 (1H, d, J=8.4), 7.52 (1H, d, J=1.8). 3-Bromo-4-(N,N-dimethylsulfamoyl)benzyl chloride (OBS02003)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098343B2
Source datasetuspto-grants-2006_08
ORD IDord-9485af3a607841f4825b672142d9a16a
Source noteuspto-grants-2006_08