HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Acrylate → Benzeneacetonitrile, 3-(methylthio)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | Benzeneacetonitrile, 3-(methylthio)- | HCID 11094968 | — |
| Reactant | 3-(Methylthio)benzyl alcohol | HCID 12255742 | — |
| Product | Benzeneacetonitrile, 3-(methylthio)- | HCID 11094968 | — |
| Product | 1-(3-Methylsulfanylphenyl)-4-oxocyclohexanecarbonitrile | HCID 59442583 | — |
Reaction Steps
The title compound was prepared according to the process described in Example 183 via the intermediates (3-methylsulfanylphenyl)methanol (MS (ESI+): 155) and (3-methylsulfanylphenyl)acetonitrile (MS (ESI+): 164). In step c), the reaction mixture was not heated under reflux after the addition of the methyl acrylate, but stirred for 16 h at room temperature. From 2.9 g of (3-methylsulfanylphenyl)acetonitrile, 0.85 g of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076324B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-735915b8a367466aa027bfc4dac26fed |
| Source note | uspto-grants-2011_12 |