HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2,5-Dichlorophenylthioacetyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178418334 | HCID 178418334 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,5-Dichlorophenylthioacetyl chloride | HCID 21716262 | 106.5% |
Reaction Steps
A solution of 2,5-dichlorophenylthioacetic acid (13.0 g, 54.9 mmol) in methylene chloride (55 mL) and thionyl chloride (10 mL, 137 mmol) was heated at reflux for 3 h. The reaction mixture was allowed to cool to room temperature and was concentrated in vacuo. The residue was evaporated two times from toluene to give 14 g of 2,5-dichlorophenyl-thioacetyl chloride (100% yield) as a slightly colored product which was used in the next step without purification. 1H NMR (300 MHz, CDCl3) δ4.13 (s, 2H), 7.22 (dd, J=2, 9 Hz, 1H), 7.35 (d, J=9 Hz, 1H), 7.39 (d, J=2 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05734047 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-6efe1ee7b8454d5381cd919bc39975fa |
| Source note | uspto-grants-1998_03 |