HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 4-Hydroxy-7-methoxy-3-(4-methoxyphenyl)-3-methylthiochroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 10979954 | HCID 10979954 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Hydroxy-7-methoxy-3-(4-methoxyphenyl)-3-methylthiochroman | HCID 22033353 | 84.2% |
Reaction Steps
To a solution of 7-methoxy-3-(4-methoxyphenyl)-3-methylthiochroman-4-one (6.29 g, 20 mmol) in THF (20 ml) and EtOH (10 ml) was added NaBH4 (1.51 g, 40 mmol), which was stirred overnight at room temperature. The reaction solution was added saturated aqueous NH4Cl solution, extracted with CHCl3, and washed with brine. The organic layer was dried over Na2SO4 and the solvent was removed under reduced pressure. The residue was purified by recrystallization with CHCl3-hexane to give 5.33 g (84%) of 4-hydroxy-7-methoxy-3-(4-methoxyphenyl)-3-methylthiochroman.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074819B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-7b71317802264f7b9f5ec3409093907e |
| Source note | uspto-grants-2006_07 |