HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 20161746, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzeneacetonitrile, 4-bromo-α,α-dimethyl-3-nitro- | HCID 20161764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20161746 | HCID 20161746 | 71.4% |
Reaction Steps
A mixture of thiophenol (9.09 g 0.0826 m), 2-methyl-2-(3-nitro-4-bromophenyl)propionitrile (18.68 g, 0.0694 m), sodium carbonate (16.0 g, 0.151 m) and absolute ethanol (300 ml) was stirred and heated at reflux for 5 hours. The cooled mixture was then poured onto ice-water and the resultant yellow solid filtered off. The crude solid was slurried with water/SVM (1.1, 300 ml) and the solid filtered and mixed with water/SVM (1:1, 150 ml. The solid was crystallised from methanol to give yellow needles (14.78 g, 65%) mpt. 146°-147° C. Calcd., for C16H14N2SO2 : C, 64.4 H, 4.7 N, 9.4; S, 10.7 Found: C, 64.5; H, 4.6; N, 9.3; S, 10.8
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04705854 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-1262a6b5b57b489cb49ee4adbfe2c3b4 |
| Source note | uspto-grants-1987_11 |