HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloromethyl methyl sulfide → (+)[N-(Benzyloxycarbonyl)morphinan-3-yloxy]methyl methyl sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloromethyl methyl sulfide | HCID 16916 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-hydroxy-N-(benzyloxycarbonyl)morphinan | HCID 53851190 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | (+)[N-(Benzyloxycarbonyl)morphinan-3-yloxy]methyl methyl sulfide | HCID 67519161 | 26% |
Reaction Steps
To Sodium hydride (763 mg of 60% dispersion in mineral oil, 19.1 mmol) in HMPA (15 mL) was added a solution of (+)-3-hydroxy-N-(benzyloxycarbonyl)morphinan (6.00 g, 15.9 mmol) from Example 1 in HMPA (50 mL) at room temperature. The reaction mixture was stirred for 30 min and then chloromethyl methyl sulfide (1.60 mL, 19.1 mmol) was added dropwise. The reaction mixture was stirred vigorously at room temperature overnight. The product was extracted with EtOAc (500 mL). The EtOAc layer was washed with saturated NaHCO3 solution and dried over MgSO4, filtered and evaporated under vacuum to provide the crude product, which was further purified by prep reverse-phase HPLC to afford the title compound (1.78 g, 26%) as a yellow gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08178551B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-50b87131f6e64864906f12ea4d863030 |
| Source note | uspto-grants-2012_05 |