HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Chlorothiophenol → 3-[(4-Chlorophenyl)thio]-azacycloheptan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3-Bromoazepan-2-one | HCID 11030635 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-[(4-Chlorophenyl)thio]-azacycloheptan-2-one | HCID 13268904 | — |
Reaction Steps
54 g (1.0 mol) of sodium methylate and 144.6 g (1.0 mol) of 4-chlorothiophenol are initially introduced into 500 mL of methanol, and a methanolic solution of 192 g (1.0 mol) of α-bromocaprolactam is added dropwise at room temperature. After the exothermic reaction has ceased, the mixture is stirred for a further 3 hours at room temperature, the precipitated sodium bromide is then filtered off under suction and the mother liquor is evaporated down in vacuo. The precipitated crystals are filtered off under suction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04468392 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-c7b72039f4ed450ca9110350fd3d7b5e |
| Source note | uspto-grants-1984_08 |