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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357324Generated: November 1, 2026

Hydrochloric Acid → Ethanethioic acid, S-(2-(acetylamino)ethyl) ester

https://huagongshe.com/reaction/1357324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantCysteamineHCID 6058—
ReactantAcetic AnhydrideHCID 7918—
ReactantCysteamine HydrochlorideHCID 9082—
ReactantPotassium HydroxideHCID 14797—
SolventWaterHCID 962—
ProductEthanethioic acid, S-(2-(acetylamino)ethyl) esterHCID 1499797%

Reaction Steps

Cysteamine hydrochloride (50.0 g) is added to a 1 L 3-neck round bottom flask fitted with a magnetic stir bar, 2 addition funnels, and a pH electrode. Water (300 mL) is added, and the stirred solution is cooled on ice. The pH is adjusted to 8.0 by addition of 8 N KOH. Acetic anhydride (125 mL) is placed in one addition funnel, and 8N KOH (350 mL) is placed in the other addition funnel. The acetic anhydride is added dropwise to the cysteamine solution, with 8 N KOH being added so as to keep the reaction pH at 8+/−1. After addition of acetic anhydride is complete, the pH was adjusted to 7.0 using 1 N HCl and the mixture is allowed to stir for 75 min. on ice. Solid NaCl is added to saturation, and the solution is extracted 4 times using 400 mL portions of CH2Cl2. The organic extracts are combined, dried over MgSO4, filtered, and concentrated under reduced pressure to yield 68.9 g (97% yield) of a pale yellow oil, which crystallizes upon standing at 4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06590083B1
Source datasetuspto-grants-2003_07
ORD IDord-b52a16d258be41b591c2feca09d77a95
Source noteuspto-grants-2003_07