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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754301Generated: October 28, 2026

Benzyl Bromide → methyl 3-(4-benzyloxyazepan-1-yl)Sulfonyl-4-bromo-benzoate

https://huagongshe.com/reaction/1754301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 4-bromo-3-(4-hydroxyazepan-1-yl)sulfonyl-benzoateHCID 118222058—
SolventDimethylformamideHCID 6228—
Productmethyl 3-(4-benzyloxyazepan-1-yl)Sulfonyl-4-bromo-benzoateHCID 11822207044.71%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a mixture of methyl 4-bromo-3-(4-hydroxyazepan-1-yl)sulfonyl-benzoate (1.00 g, 2.55 mmol, 1.00 Eq) in DMF (15 mL), was added NaH (153.00 mg, 3.82 mmol, 1.50 Eq) in portions at 0° C. under N2. The mixture was stirred at 25° C. for 30 min. Then bromomethylbenzene (654.19 mg, 3.82 mmol, 1.50 Eq) was added and stirred at 25° C. for 16 hours. TLC showed the reaction was completed. The mixture was poured into NH4Cl aqueous and extracted with EA. The combined organic phase was washed with saturated brine, dried with anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by silica gel chromatography (eluting with PE/EA=10/1, 2/1) to afford methyl 3-(4-benzyloxyazepan-1-yl)Sulfonyl-4-bromo-benzoate (550.00 mg, 1.14 mmol, 44.71% yield) as white solid. LCMS: 482/484 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169212B2
Source datasetuspto-grants-2015_10
ORD IDord-a85a2fe59f554313bd67671f80530831
Source noteuspto-grants-2015_10