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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 4-bromo-3-(4-hydroxyazepan-1-yl)sulfonyl-benzoate | HCID 118222058 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 3-(4-benzyloxyazepan-1-yl)Sulfonyl-4-bromo-benzoate | HCID 118222070 | 44.71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169212B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-a85a2fe59f554313bd67671f80530831 |
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| Source note | uspto-grants-2015_10 |
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