HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924437Generated: November 1, 2026
Sulfuryl chloride → (+)-[N-(benzyloxycarbonyl)morphinan-3-yloxy]methyl chloride
https://huagongshe.com/reaction/1924437
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | (+)[N-(Benzyloxycarbonyl)morphinan-3-yloxy]methyl methyl sulfide | HCID 67519161 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+)-[N-(benzyloxycarbonyl)morphinan-3-yloxy]methyl chloride | HCID 67519222 | — |
Reaction Steps
To (+)[N-(Benzyloxycarbonyl)morphinan-3-yloxy]methyl methyl sulfide (1.78 g, 4.07 mmol) in DCM (40 mL) was added sulfuryl chloride (6.1 mL, 6.11 mmol) at room temperature. The reaction mixture was stirred at room temperature overnight. After removal of excess reagent and DCM by rotary evaporation, the product was dried under vacuum to afford (+)-[N-(benzyloxycarbonyl)morphinan-3-yloxy]methyl chloride as a yellow gum. Then, it was added to a stirred suspension of cesium carbonate (1.59 g, 4.88 mmol) and isobutyric acid (0.45 mL, 4.88 mmol) in acetone (20 mL) at room temperature. The reaction mixture was stirred at room temperature overnight. After the reaction was completed, the reaction mixture was filtered and evaporated under vacuum to provide the crude product, which was further purified by prep reverse-phase HPLC to afford the title compound (0.844 g, 43%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178551B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-4fdf9d5bb20f4e0f97f41747f8d98045 |
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| Source note | uspto-grants-2012_05 |
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