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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175365Generated: October 29, 2026

Acetic Acid → Oxycodone Hydrochloride

https://huagongshe.com/reaction/2175365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantOxycodoneHCID 5284603—
SolventWaterHCID 962—
ProductOxycodone HydrochlorideHCID 546235096.4%

Reaction Steps

Purified oxycodone base (19.22 g, 60.95 mmol, Lot S) and a mixture of water (28.83 g) and acetic acid (2.82 g, 16.19 mmol/g, 44.70 mmol) were charged into 150-mL RBF, equipped with mechanical stirrer. Stirring of the mixture at ambient temperature (230 RPM) resulted in a thin suspension formation. Hydrochloric acid (6.94 g, 10.094 mmol/g, 70.09 mmol) was added portion-wise over 45 minutes: at the beginning—about 2.30 g (over ˜4 minutes, the mixture became transparent, followed by a precipitation); the rest of the hydrochloric acid was added portion-wise (5 drops at once) over 40 minutes (rate of stirring was increase to 250 RPM after 30 minutes). The mixture was stirred for 0.5 hours at ambient temperature, 0.5 hours at ice-bath temperature, and cold IPA (0° C., 77 mL) was added over 25 minutes. Stirring continued for 0.5 hours, and the precipitated product was filtered off. It was washed with IPA (2×40 mL) and acetone (2×40 mL), dried on filter providing 21.73 g (58.76 mmol, 96.4% yield) of oxycodone HCl crystalline white solids, Lot T. Impurity profiles of materials of interest were monitored by HPLC, normalization method, as shown in Table 10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062062B1
Source datasetuspto-grants-2015_06
ORD IDord-c3143deb1354424b8f9dfc1ab22cd1b3
Source noteuspto-grants-2015_06