Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966132Generated: October 26, 2026

Hydrochloric Acid → Dihydrolipoic Acid

https://huagongshe.com/reaction/966132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantalpha Lipoic acidHCID 864—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantSodiumHCID 5360545—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
ProductDihydrolipoic AcidHCID 421100%

Reaction Steps

6,8-Bismercaptooctancoic acid: α-Lipoic acid (5.15 g, 25.0 mmol) was suspended in 125 mL of water and sodium bicarbonate (2.10 g, 25.0 mmol) added. The mixture was sonicated to generate the sodium salt. The resulting pale yellow solution was cooled in an ice bath and solid sodium borohydride (1.90 g, 50.0 mmol) added with stirring in small portions over 20 min. The solution was stirred at ice bath temperature another 30 min, and then at room temperature for 30 min. The cloudy solution was cooled in an ice bath, and the pH brought to about 1 by the slow addition of 2M hydrochloric acid. A vigorous evolution of hydrogen occurred as the excess sodium borohydride decomposed and an oily liquid separated. As much as possible the following operations were performed under nitrogen. The mixture was extracted with 3×50 mL of chloroform. The combined chloroform extracts were dried over magnesium sulfate, filtered and the solvent evaporated under reduced pressure at room temperature. The oil remaining was further dried under vacuum to remove the last traces of solvent. The 6,8-bismercaptooctanoic acid was isolated as a colorless oil weighing 5.2 g (100% yield). The product was stored at −20° under nitrogen.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951887B2
Source datasetuspto-grants-2005_10
ORD IDord-6e2262c4555b438c8aed68e3c187fa2b
Source noteuspto-grants-2005_10