Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118346Generated: October 31, 2026

N-(5-Acetyl-2-benzyloxyphenyl)-N-benzylmethanesulfonamide → N-Benzyl-N-[2-benzyloxy-5-(2-bromoacetyl)phenyl]methanesulfonamide

https://huagongshe.com/reaction/2118346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-Acetyl-2-benzyloxyphenyl)-N-benzylmethanesulfonamideHCID 12363924—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventTetrahydrofuranHCID 8028—
ProductN-Benzyl-N-[2-benzyloxy-5-(2-bromoacetyl)phenyl]methanesulfonamideHCID 86607679—

Reaction Steps

A solution of N-{5-acetyl-2-[(phenylmethyl)oxy]phenyl}-N-(phenylmethyl) methanesulfonamide (J. Med Chem 1977, 20, 687-92) (1.18 g) in THF (50 ml) was treated with phenyltrimethylammonium tribromide (1.08 g) at <10° and stirred for 6 h. The reaction mixture was quenched with chilled water and then filtered. The filtrate was partitioned between diethyl ether and water, the organic phase was dried (MgSO4) and the solvent was removed in vacuo. The mixture was purified by column chromatography on silica (SPE bond elut, gradient 0 to 45% EtOAc-cyclohexane) to afford the title compound. LCMS RT=3.48 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442839B2
Source datasetuspto-grants-2008_10
ORD IDord-8a5d6ff9f23c4a2b82f3ef71fd30b183
Source noteuspto-grants-2008_10