HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Bromo-2-nitrotoluene → HCID 23199182, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Bromo-2-nitrotoluene | HCID 77569 | — |
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23199182 | HCID 23199182 | — |
Reaction Steps
164 a) A suspension of o-Nitrobenzylbromide (5.71 g, 26.4 mmol) and sodium methanesulfinate (4.0 g, 40.0 mmol) in ethanol (70 mL) was stirred at room temperature for 18 hours. The volatiles were evaporated under reduced pressure. To the residue was added water (50 mL) and stirred for 30 minutes. The suspension was filtered, rinsed with water and air dried. 1-Methanesulfonylmethyl-2-nitro-benzene was isolated as a yellow solid (5.36 g, 94%). MP=115-117° C. 1H NMR (400 MHz, CDCl3, δ, ppm): 8.10 (d, J=8.1 Hz, 1H), 7.74-7.65 (m, 2H), 7.62-7.58 (m, 1H), 4.80 (s, 2H), 2.91 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633173B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-cce21671c7c7436197cc311dd9890c0d |
| Source note | uspto-grants-2014_01 |