HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 5-(Triphenylmethyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,5,6,7-Tetrahydrothieno(3,2-c)pyridine | HCID 3085076 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(Triphenylmethyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine | HCID 13748461 | — |
Reaction Steps
20 cm3 (0.079 mole) of triethyl amine are added dropwise to the solution of 10 g (0.072 mole) of 4,5,6,7-tetrahydro-thieno[3,2-c]pyridine and 20 cm3 of dichloro methane at room temperature and 20.02 g (0.072 mole) of triphenyl-methyl-chloride are added. The reaction mixture is kept at room temperature for a night and is poured onto 200 cm3 of water. The phases are separated; the organic phase is dried on sodium sulfate and evaporated to dryness. The residual product is purified by silica gel chromatography using dichloro methane as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169265B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-f9ee713adb8e4f7e8e46a54f759eb436 |
| Source note | uspto-grants-2015_10 |