Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Benzonitrile, 3-(bromomethyl)- | HCID 97249 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 60754457 | HCID 60754457 | — |
Reaction Steps
To a solution of 3-bromomethyl-benzonitrile (2 g, 10.2 mmol) in EtOH (50 mL) is added a solution of Na2SO3 (1.3 g, 10.3 mmol) in H2O (50 mL) and the mixture is heated at reflux for 4 hours. The mixture is concentrated in vacuo. The residue is suspended in DCM (100 mL) and DMF (1 mL), cooled to 0° C. and treated with oxalyl chloride (4.5 mL, 24.4 mmol). The mixture is warmed to room temperature for 3 hours. The mixture is diluted with brine (100 mL), extracted with DCM (2×100 mL), dried with Na2SO4, filtered, and concentrated in vacuo. The residue is dissolved in THF (100 mL), and treated with isopropyl amine (3.5 mL, 40.8 mmol). The mixture is stirred for 12 h, diluted with EtOAc (200 mL), washed with saturated aqueous NH4Cl (2×100 mL), dried with Na2SO4, filtered, and concentrated in vacuo. The residue is purified by flash chromatography eluting with 20%-80% EtOAc/heptane to afford C-(3-cyano-phenyl)-N-isopropyl-methanesulfonamide as a powder. MS: 237 (M+H); 1H NMR (300 MHz, DMSO-d6): δ 1.10 (d, J=6.6 Hz, 6H), 3.36 (m, 1H), 4.42 (s, 2H), 7.09 (m, 1H), 7.57 (m, 1H), 7.74 (m, 1H), 7.85 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202863B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-9d393fa9fddb4fe69933fbcd08a3dbc5 |
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| Source note | uspto-grants-2012_06 |
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