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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696840Generated: October 31, 2026

Sodium Bicarbonate → N-Benzyl-N-[2-benzyloxy-5-(2-bromoacetyl)phenyl]methanesulfonamide

https://huagongshe.com/reaction/1696840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantN-(5-Acetyl-2-benzyloxyphenyl)-N-benzylmethanesulfonamideHCID 12363924—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventTetrahydrofuranHCID 8028—
ProductN-Benzyl-N-[2-benzyloxy-5-(2-bromoacetyl)phenyl]methanesulfonamideHCID 8660767985%

Reaction Steps

Phenyltrimethylammonium tribromide (1.19 g, 3.16 mmol) was added to a solution of N-(5-acetyl-2-benzyloxyphenyl)-N-benzylmethanesulfonamide (32) (1.23 g, 3.01 mmol) in anhydrous THF (15 mL) in three portions. The reaction mixture was stirred at rt for 16 h. An aqueous sodium bicarbonate solution (5%, 15 mL) was then added. The mixture was extracted with dichloromethane and combined organics were concentrated by rotary evaporation. The resulting residue was purified by Biotage silica gel column chromatography eluting with dichloromethane to give bromo ketone 33 as a solid (1.25 g, 85% yield): 1H NMR (500 MHz, CDCl3) δ 2.85 (s, 3H), 4.21 (s, 2H), 4.75 (br, 2H), 5.19 (s, 2H), 7.08 (d, 1H), 7.22 (m, 5H), 7.43 (m, 5H), 7.65 (d, 1H), 7.92 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163758B2
Source datasetuspto-grants-2012_04
ORD IDord-9879d8b0080e468983b71eab37cd290a
Source noteuspto-grants-2012_04