HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluorotoluene-alpha-thiol → benzyl 3-(4-fluorobenzylthio)-N-phenyl-thioacrylimidate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluorotoluene-alpha-thiol | HCID 85171 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Benzyl N-phenylpropynthioimidate | HCID 86617334 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | benzyl 3-(4-fluorobenzylthio)-N-phenyl-thioacrylimidate | HCID 86617333 | — |
Reaction Steps
Benzyl N-phenylpropynthioimidate (0.30 g) and 4-fluorobenzylmercaptan were dissolved to chloroform (15 ml), catalytic amount of potassium t-butoxide was added thereto under ice-cooling and stirred at room temperature for 14 hours. The reaction mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=15:1) to obtain benzyl 3-(4-fluorobenzylthio)-N-phenyl-thioacrylimidate (0.15 g) as light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084644B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-ceb10f6f62264911a8fb5cbfff922df2 |
| Source note | uspto-grants-2011_12 |