HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Chlorothiophenol → Methyl alpha-(p-chlorophenylthio)-alpha-[p-(p-chlorophenoxy)phenyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | Methyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetate | HCID 20392594 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl alpha-(p-chlorophenylthio)-alpha-[p-(p-chlorophenoxy)phenyl]acetate | HCID 20392626 | — |
Reaction Steps
Methyl α-bromo-α-[p-(p-chlorophenoxy)phenyl]acetate (7.11 g) is reacted with 3.61 g of 4-chlorothiophenol in methanol, as in Example 16, to give a yellow oil which is bulb distilled at 0.01 mm to afford colorless oil (188° C) which solidifies to give white crystals, mp 71°-75° C. A portion is recrystallized from hexane to give white nedles, mp 74°-75.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125729 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-86ad3fe8552b4dd88975487d13014ed0 |
| Source note | uspto-grants-1978_11 |