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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352392Generated: October 30, 2026

Benzyl Bromide → HCID 563866, compound

https://huagongshe.com/reaction/352392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 2055080HCID 2055080—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 563866HCID 56386665.1%

Reaction Steps

Part A: To a solution of 10.04 g (43 mmol) of N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide from Example 1 in 85 mL of anhydrous DMF, was added 17.8 g (128 mmol) of powdered potassium carbonate and then 8.2 g (48 mmol) of benzyl bromide. After 24 hours, ethyl acetate and water was added, the organic layer separated and washed 3×s with brine, dried with sodium sulfate, filtered and stripped to afford 14.3 g of crude product. This was recrystallized from tert-butylmethyl ether/hexane to afford 9.0 g of the desired N-(hydroxyethyl)-N-(phenylmethyl)-4-methoxybenzene-sulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747027B1
Source datasetuspto-grants-2004_06
ORD IDord-f1129cbf9ebe46dda3fa444aef953ab8
Source noteuspto-grants-2004_06