HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128207Generated: October 25, 2026
Ethanolamine → 2-(Bis(2-hydroxyethyl)amino)ethanesulphonic acid
https://huagongshe.com/reaction/128207
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium bromoethanesulfonate | HCID 23705444 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Bis(2-hydroxyethyl)amino)ethanesulphonic acid | HCID 73243 | — |
Reaction Steps
A solution of 90 g of sodium bromoethanesulphonate (Organic Synthesis, Coll. Vol. II, p; 558) and 110 g of ethanolamine in 1500 ml of water was heated over a steam bath for about 2 hours and the reaction mixture left to stand for one night. The excess diethanolamine and water were then distilled off under vacuum, and the residue taken up in 100 ml of water and 800 ml of concentrated hydrochloric acid. The solution was cooled and filtered from the sodium chloride by a filter pump. It was then concentrated under vacuum until an oil was obtained which was taken up in boiling ethanol. On cooling, a crystalline product was obtained having a melting point of 163°-165° C., which was recrystallised from ethanol and water. 16 G of product were obtained, the analytical and spectroscopic data of which confirmed the identity of the product as the compound (III).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04259332 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-d1c4e63bcd184144bf099f58d9a8b652 |
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| Source note | uspto-grants-1981_03 |
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