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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168186Generated: October 31, 2026

Allyl bromide → Naloxone

https://huagongshe.com/reaction/2168186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTriethylamineHCID 8471—
Reactant14-Hydroxymorphine-6-oneHCID 15286253—
SolventDichloromethaneHCID 6344—
SolventN-methylpyrrolidone-waterHCID 22287110—
ProductNaloxoneHCID 528459684.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

Allyl bromide (56 mg; 0.463 mmol) and Et3N (45 μl; 0.327 mmol) were added to a suspension of noroxymorphone (Example 5, 100 mg; 0.348 mmol) in a mixture of NMP/H2O (10:1; 0.35 mL). The reaction vessel was purged with argon and the mixture was stirred at 70° C. for 2 h. At that time, additional Et3N (45 μl; 0.327 mmol) was added and the mixture was stirred for an additional 7.5 h at 70° C. The reaction mixture was then cooled to room temperature, diluted with dichloromethane (15 mL), and washed with saturated NaHCO3 (3×3 mL). The aqueous layer was re-extracted with dichloromethane (5 mL) and the combined organic layers were dried over MgSO4. Column chromatography of the residue (dichloromethane/methanol 4:1) afforded 96 mg (84%) of naloxone as a white solid mp: 181-182° C. (ethyl acetate), [lit. mp 173-175]xix [lit. 179.5° C. (toluene)]xx identical in all respects to the material described in the literature.xxi

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045497B1
Source datasetuspto-grants-2015_06
ORD IDord-29adc877c2fa4e2e867f1204b482daa4
Source noteuspto-grants-2015_06