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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924436Generated: November 1, 2026

Chloromethyl methyl sulfide → (+)[N-(Benzyloxycarbonyl)morphinan-3-yloxy]methyl methyl sulfide

https://huagongshe.com/reaction/1924436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl methyl sulfideHCID 16916—
ReactantSodium hydrideHCID 24758—
Reactant3-hydroxy-N-(benzyloxycarbonyl)morphinanHCID 53851190—
SolventHexamethylphosphoramideHCID 12679—
Product(+)[N-(Benzyloxycarbonyl)morphinan-3-yloxy]methyl methyl sulfideHCID 6751916126%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178551B2
Source datasetuspto-grants-2012_05
ORD IDord-50b87131f6e64864906f12ea4d863030
Source noteuspto-grants-2012_05