HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 2,2-dimethyl-6-[(4-phenyl-2-quinolyl)thio]-hexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-4-phenylquinoline | HCID 2306687 | — |
| Reactant | Methyl 2,2-dimethyl-6-mercaptohexanoate | HCID 15681404 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2,2-dimethyl-6-[(4-phenyl-2-quinolyl)thio]-hexanoate | HCID 10318437 | — |
Reaction Steps
To a solution of 4 g of methyl 2,2-dimethyl-6-mercaptohexanoate in 100 cc of dimethylformamide, is added 0.55 g of sodium hydride (50% w/w dispersion in mineral oil). The mixture is stirred for 2 hours until effervescence has stopped. A solution of 5 g of 2-chloro-4-phenylquinoline in 50 cc of dimethyl-formamide is then added. The obtained mixture is heated to 60 C. for 8 hours. After cooling, 10 cc of methanol is added and the mixture evaporated. The resultant residue is purified by flash chromatography on silica gel (30-60 mm; eluent: 8:2 hexane/ethyl acetate) to give methyl 2,2-dimethyl-6-[(4-phenyl-2-quinolyl)thio]-hexanoate is obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05492915 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-23144e7c724a4dbaa012d25b027155a3 |
| Source note | uspto-grants-1996_02 |