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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040747Generated: October 25, 2026

Hydrochloric Acid → Naltrexone

https://huagongshe.com/reaction/2040747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-ethyl-2-pyrrolidoneHCID 17595—
ReactantBromomethylcyclopropaneHCID 81503—
ReactantDiisopropylethylamineHCID 81531—
Reactant14-Hydroxymorphine-6-oneHCID 15286253—
SolventWaterHCID 962—
ProductNaltrexoneHCID 5360515100.1%

Reaction Conditions

Temperature54.5 °C

Reaction Steps

A mixture of noroxymorphone (60 Kg, 0.209 Kmol), N-ethyl-2-pyrrolidinone (180 kg), cyclopropymethyl bromide (36.6 kg) and N,N-diisopropylethylamine (35.1 kg) was heated to 52-57° C. for 20 hours and 10 minutes. The mixture was then diluted with a solution prepared by mixing hydrochloric acid 37% (29 kg) and water (79 kg). Low boiling compounds were removed by distillation under vacuum keeping the temperature below 70° C. After cooling to 25-30° C. the mixture was further diluted with water (1910 kg). Ammonium hydroxide 4% (199 kg) was then added over three hours till pH=9-10 to precipitate the product. The solid was filtered, washed with water (2×120 kg) and dried under vacuum at 60° C. obtaining 68.5 kg of naltrexone (molar yield 93.2%). HPLC analysis (% by area): naltrexone 99.1%, noroxymorphone 0.11%, 3-cyclopropylmethylnaltrexone 0.41%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580963B2
Source datasetuspto-grants-2013_11
ORD IDord-a7a23e5c317b4a429759676c009ad4f9
Source noteuspto-grants-2013_11