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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant(+)[N-(Benzyloxycarbonyl)morphinan-3-yloxy]methyl methyl sulfideHCID 67519161—
SolventDichloromethaneHCID 6344—
Product(+)-[N-(benzyloxycarbonyl)morphinan-3-yloxy]methyl chlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178551B2
Source datasetuspto-grants-2012_05
ORD IDord-4fdf9d5bb20f4e0f97f41747f8d98045
Source noteuspto-grants-2012_05