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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827595Generated: October 30, 2026

Sodium Bicarbonate → N-(2-chloro-4-hydroxy-benzyl)-N-[4-(3-hydroxy-propyl)-phenyl]-2,4,6-trimethyl-benzenesulfonamide

https://huagongshe.com/reaction/1827595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantN-(2-chloro-4-hydroxy-benzyl)-2,4,6-trimethyl-N-[4-(3-oxo-propyl)-phenyl]-benzenesulfonamideHCID 22137388—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductN-(2-chloro-4-hydroxy-benzyl)-N-[4-(3-hydroxy-propyl)-phenyl]-2,4,6-trimethyl-benzenesulfonamideHCID 2213735047.5%

Reaction Steps

To a solution of N-(2-chloro-4-hydroxy-benzyl)-2,4,6-trimethyl-N-[4-(3-oxo-propyl)-phenyl]-benzenesulfonamide (0.036 g, 0.08 mmol) in 0.2 mL methanol and 0.2 mL methylene chloride was added sodium borohydride (0.014 g, 0.38 mmol). The reaction mixture was stirred at room temperature for 24 hr. Saturated aqueous sodium bicarbonate was added and the aqueous solution was washed with methylene chloride. The organic layer was dried (magnesium sulfate) and concentrated. Medium pressure silica gel chromatography (40% ethyl acetate/hexanes) afforded 0.018 g of N-(2-chloro-4-hydroxy-benzyl)-N-[4-(3-hydroxy-propyl)-phenyl]-2,4,6-trimethyl-benzenesulfonamide. MS 474.0 (M+1)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053212B2
Source datasetuspto-grants-2006_05
ORD IDord-d2edf6000da34aef9f243e7a0ad0698c
Source noteuspto-grants-2006_05