HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethynyl-4-fluorobenzene → Z-4-fluorostyryl 2-chlorobenzylsulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethynyl-4-fluorobenzene | HCID 522627 | — |
| Reactant | 2-Chlorobenzyl mercaptan | HCID 580759 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | Z-4-fluorostyryl 2-chlorobenzylsulfide | HCID 86588942 | — |
Reaction Steps
A solution of 4-fluorophenylacetylene (0.02 mol) and 2-chlorobenzyl mercaptan (0.02 mol) and metallic sodium (0.02 g atom) was subjected to Procedure 2 to form (Z)-4-fluorostyryl 2-chlorobenzylsulfide. The title compound was obtained in 74% yield following oxidation. 1HNMR (CDC13) δ4.55 (2H, s), 6.66 (1H, d, JH,H=11.94), 7.20-7.65 (8H aromatic+1H ethylenic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06767926B1 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-fa6c3a3b9c174fc3b85341b248261eec |
| Source note | uspto-grants-2004_07 |