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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868433Generated: October 30, 2026

Chloride → Gabapentin hydrochloride

https://huagongshe.com/reaction/1868433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantGabapentinHCID 3446—
ProductGabapentin hydrochlorideHCID 6453919—

Reaction Steps

is dissolved in chloride free demineralized water (375 ml) at 50 degrees. The solution is treated with charcoal at the same temperature and filtered through a bed of hyflo. The bed is washed with demineralized water (150 ml). The filtrate is cooled to 10 deg and neutralized with sodium lye (110 g of 50% w/w sodium hydroxide solution) with the temperature kept strictly below 15 degrees. The neutralized mixture is heated to 70-75 degrees over a period of 3 hours to get a clear solution, then cooled to 5-10 degrees over a period of 4 hours and kept at that temperature range for 1 hr and filtered (mother liquor A). The product is suck dried thoroughly to give moist gabapentin (about 195 g) having water content of 14%. This is dissolved in a mixture of methanol (570 ml) and water (60 ml) at about 70 degrees. The solution is treated with activated charcoal (5 g) and filtered through a bed of hyflo. The bed is washed with a mixture of methanol (80 ml) and water (16 ml). To the combined filtrates is added isopropanol (815 ml). The mixture is cooled to 0-5 degrees and maintained for 1 hr, when pure white gabapentin crystallizes out, the mixture is centrifuged; the product is spin-dried for 45 min (mother liquor B) and dried to yield gabapentin (125 g) with 1. Chloride 40 ppm, 2. Gabalactam, 0.01%, 3. Impurity with RF 0.5 relative to gabapentin NIL 4. Any other individual impurity less than 0.1% 5. Total impurities 0.032%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635717B2
Source datasetuspto-grants-2009_12
ORD IDord-48c76800507249a9a2993c5ab92d30dc
Source noteuspto-grants-2009_12