Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-[4-(Hydroxymethyl)phenoxy]benzene-1,2-dicarbonitrile | HCID 68695134 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11449786 | HCID 11449786 | 92% |
Reaction Steps
To a solution of 4-[4-(hydroxymethyl)phenoxy]phthalonitrile (1.0 g, 3.9 mmol) prepared according to procedures described in literature, and triethylamine (0.80 ml, 5.8 mmol) in anhydrous CH2Cl2 (50 ml), kept at 0° C. under stirring and in an inert atmosphere, methylsulfonylchloride was added (0.33 ml, 4.3 mmol). The mixture was stirred at 0° C. for 1 hour, then ft was diluted with CH2Cl2 (50 ml) and washed with 1% HCl solution (60 ml), then with brine (50 ml), the organic layer was dried on Na2SO4 and the solvent was evaporated. 1.2 g (92%) of the title compound were obtained as a viscous fluid that crystallised on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842682B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-dcf436c464f9447b86fdeff21e3687ec |
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| Source note | uspto-grants-2010_11 |
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