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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874057Generated: October 27, 2026

Hydrochloric Acid → HCID 15250630, compound

https://huagongshe.com/reaction/874057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,2-EthanedithiolHCID 10902—
ReactantSodium MethoxideHCID 10942334—
Reactant2-Bromoethanesulfonic acid, sodium saltHCID 23666797—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 15250630HCID 1525063064.6%

Reaction Steps

To a solution of 2-bromoethylsulfonate sodium salt (25.6 g, 125 mmol) and sodium methoxide (8.03 g, 149 mmol) in EtOH (350 mL) at 0° C. was added, dropwise, a solution of 1,2-ethanedithiol (5.00 mL, 59.4 mmol) in EtOH (25 mL). The reaction mixture was allowed to warm to room temperature, and then heated to reflux for 48 hours. Next, the mixture was cooled to room temperature, and then acidified with 2 N HCl to pH 1-2. The resulting suspension was heated to 75° C. and water was slowly added in small portions until a clear solution was obtained. The reaction mixture was then cooled to room temperature, and then to 5° C. The resulting white precipitate was filtered off, washed with cold EtOH and dried, giving 11.9 g (64.6%) of Compound 4 as a white powder. 1H NMR (500 MHz, D2O) δ 3.27 (t, J=9.3, 6.4 Hz, 4H), 3.06-2.99 (m, 4H), 2.98 (s, 4H). 13C NMR (126 MHz, D2O) δ 51.11, 31.09, 25.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980077B2
Source datasetuspto-grants-2015_03
ORD IDord-8624df889ae14d37aaf9fb2ab4ccde9c
Source noteuspto-grants-2015_03