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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962396Generated: October 31, 2026

Sodium Hydroxide → N-(2-(acetylthio)ethyl)-N-(3-carboxy-3-hydroxy-3-phosphonopropyl)-N,N-dimethylammonium bromide

https://huagongshe.com/reaction/962396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthanethioic acid, S-(2-bromoethyl) esterHCID 523036—
Reactant4-(N,N-dimethylamino)-2-hydroxy-2-phosphonobutanoic acidHCID 19084804—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductN-(2-(acetylthio)ethyl)-N-(3-carboxy-3-hydroxy-3-phosphonopropyl)-N,N-dimethylammonium bromideHCID 19084786—

Reaction Steps

A solution of 2.27 g (0.01 mole) of 4-(N,N-dimethylamino)-2-hydroxy-2-phosphonobutanoic acid (prepared as described in Method 1) in 20 ml water and 40 ml ethanol is adjusted to pH 7.0 by addition of 1N aqueous NaOH. To this is added 9.16 g (0.05 mole) of S-acetyl-2-bromoethanethiol, and the reaction is heated at 40°-80° for several hours. The reaction is evaporated to dryness under reduced pressure. The resulting residue is triturated with acetone several times (acetone extracts are discarded). The remaining solid is dissolved in distilled water, and is treated with cation exchange resin in H+ form. The resin is filtered off, the aqueous solution is concentrated to a few ml, and acetone is added dropwise to precipitate the product. This is purified by recrystallization from water/acetone to give N-(2-(acetylthio)ethyl)-N-(3-carboxy-3-hydroxy-3-phosphonopropyl)-N,N-dimethylammonium bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760021
Source datasetuspto-grants-1998_06
ORD IDord-70229989750548c9970e601333aca494
Source noteuspto-grants-1998_06