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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860616Generated: November 2, 2026

Gabapentin hydrochloride → Gabapentin

https://huagongshe.com/reaction/1860616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGabapentin hydrochlorideHCID 6453919—
SolventIsopropanolHCID 3776—
ProductGabapentinHCID 3446—

Reaction Conditions

Temperature40 °C

Reaction Steps

Gabapentin hydrochloride was dissolved in 130 ml dry isopropanol at 25° C. by mixing, then 1.1 g of active carbon was added and the suspension was heated to 40° C. and maintained for two hours at 40° C. The suspension was filtered at 40° C. and the filter cake was washed twice with additional 15 ml of isopropanol each time. The washings were added to the already separated solution of gabapentin hydrochloride in isopropanol. The solution was concentrated to dryness in vacuum (approximately 10 mm Hg) to constant weight. The temperature of the heating bath was maintained at maximum 35° C. during this operation. Next, 245 ml of ethylacetate was added to the dry residue of gabapentin hydrochloride and the mixing was started. After half an hour of mixing at 25° C., an amount of 28.3 grams of trihexylamine was added during half an hour and the mixing was continued for an additional two hours at the same temperature. The formed gabapentin base was separated from the suspension by filtration. The filter cake was washed with 23 ml of ethylacetate and 23 ml of methanol to give gabapentin crude. After reslurry as in Example 1B, gabapentin pure was obtained having a yield of 75.0% and chloride anion content of 213 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531509B2
Source datasetuspto-grants-2003_03
ORD IDord-cb6160f6edaf412a9fda25420e1b54ba
Source noteuspto-grants-2003_03