HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethanol, 2-[2-[2-(2-mercaptoethoxy)ethoxy]ethoxy]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Tetraethylene glycol p-toluenesulfonate | HCID 13456094 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | Ethanol, 2-[2-[2-(2-mercaptoethoxy)ethoxy]ethoxy]- | HCID 10465720 | — |
Reaction Steps
A solution of thiourea (0.94 g, 12.35 mmol) and toluene-4-sulfonic acid 2-{2-[2-(2-hydroxy-ethoxy)-ethoxy]-ethoxy)-ethyl ester (4.09 g, 11.75 mmol) in absolute alcohol (32 ml) was heated to reflux under argon atmosphere for 24 h. The mixture was cooled and a solution of NaOH (1.23 g, 30.75 mmol) in 15 ml of ethanol/water (9:1, v/v) was added. Refluxing was continued for another 2.5 h under argon. The reaction mixture was then cooled to ambient temperature and acidified to pH 2 using concentrated hydrochloric acid and then concentrated under reduced pressure. The residue was purified by flash chromatography using ethyl acetate/absolute ethanol (10:1) to afford the product as a colourless oil. Yield 1.55 g (66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368474B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-adfdeea70bd842ddbb86d9fb687995e4 |
| Source note | uspto-grants-2008_05 |