Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040749Generated: October 29, 2026

Hydrochloric Acid → Naltrexone

https://huagongshe.com/reaction/2040749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-ethyl-2-pyrrolidoneHCID 17595—
ReactantBromomethylcyclopropaneHCID 81503—
ReactantDiisopropylethylamineHCID 81531—
Reactant14-Hydroxymorphine-6-oneHCID 15286253—
SolventWaterHCID 962—
ProductNaltrexoneHCID 5360515100.8%

Reaction Conditions

Temperature54.5 °C

Reaction Steps

A mixture of noroxymorphone (62 Kg), N-ethyl-2-pyrrolidinone (186 kg), cyclopropymethyl bromide (37.8 kg) and N,N-diisopropylethylamine (36.2 kg) was heated to 52-57° C. for 24 hours and 45 min. The mixture was then diluted with a solution prepared by mixing hydrochloric acid 37% (30 kg) and water (82 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 (1975 kg). Ammonium hydroxide 4% (206 kg) was then added over three hours till pH=9-10 to precipitate the product. The solid was filtered, washed with water (2×124 kg) and dried under vacuum at 60° C. obtaining 71.3 kg of naltrexone (molar yield 89.6%). HPLC analysis (% by area): naltrexone 99.45%, noroxymorphone 0.16%, 3-cyclopropylmethylnaltrexone 0.28%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580963B2
Source datasetuspto-grants-2013_11
ORD IDord-b24d7f8899f24029884c26f6c5d6b9a7
Source noteuspto-grants-2013_11