Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057293Generated: October 31, 2026

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

https://huagongshe.com/reaction/1057293

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 numberUS06514944B2
Source datasetuspto-grants-2003_02
ORD IDord-c59426f97aae4ea88510b98fc543c838
Source noteuspto-grants-2003_02