HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → phenyl 3-methylthio-N-phenylacrylimidate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Phenyl 3-phenoxy-N-phenylacrylimidate | HCID 69127142 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | phenyl 3-methylthio-N-phenylacrylimidate | HCID 69126846 | 78.1% |
Reaction Steps
Phenyl 3-phenoxy-N-phenylacrylimidate (0.30 g) was dissolved to THF (5 ml), sodium salt of methyl mercaptan (0.075 g) was added thereto and stirred for four hours at room temperature. Ethyl acetate (50 ml) was added to the reaction solution, and it was successively washed with water and aqueous saturated of sodium chloride solution, dried over magnesium sulfate (anhydrous), concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain phenyl 3-methylthio-N-phenylacrylimidate (0.20 g) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08618329B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-c7badc4004d04c9ea4ad6879e96bcc4a |
| Source note | uspto-grants-2013_12 |