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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434521Generated: October 28, 2026

L-Tartaric acid → HCID 22042229, compound

https://huagongshe.com/reaction/434521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Tartaric acidHCID 444305—
ReactantHCID 20492819HCID 20492819—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 22042229HCID 22042229—

Reaction Steps

A 46.5 g-quantity of the above compound (free base) is dissolved in 200 ml of ethanol, and a solution of 15 g of L-tartaric acid in 200 ml of water is added to the ethanol solution. The resulting mixture is allowed to stand at room temperature. The crystals thus precipitated are recrystallized three times from ethanol-water (6:4) to give tartrate monohydrate as colorless prisms. The tartrate monohydrate is treated with an aqueous solution of sodium bicarbonate to give (-)-1-[5-(4-fluorophenyl)-4,5-dihydroisoxazol-3-ylmethyl]-4-(5-chloro-2-oxo-1-benzimidazolinyl)piperidine. Melting point: 143°-145° C. [α]D25 : -108.8 (chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04397853
Source datasetuspto-grants-1983_08
ORD IDord-87d9b87514c64c7ab521664c05549dda
Source noteuspto-grants-1983_08