HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885914Generated: November 1, 2026
4-Nitrobenzyl bromide → 1-(Methanesulfonylmethyl)-4-nitrobenzene
https://huagongshe.com/reaction/885914
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Methanesulfonylmethyl)-4-nitrobenzene | HCID 287370 | 75.3% |
Reaction Steps
To a stirred solution of 4-nitrobenzyl bromide (10.0 g, 46.3 mmol) in DMF (25 mL) was added sodium methanesulfinate (7.1 g, 69.4 mmol). The reaction mixture was stirred at 65° C. for 30 minutes, and then partitioned between water (30 mL) and EtOAc (30 mL). The organic fraction was separated, washed with water (2×30 ml), dried (Na2SO4), filtered and concentrated in vacuo to give the title compound (7.5 g, 75%) as a yellow solid that was used without further purification. δH (DMSO-d6) 8.28 (2H, d, J 8.8 Hz), 7.70 (2H, d, J 8.8 Hz), 4.72 (2H, s), 2.97 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242116B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-b147a0fcc7e64cb0bc6aaa54d6a784a6 |
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| Source note | uspto-grants-2012_08 |
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