HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85712Generated: October 30, 2026
Ethanolamine → 3-((2-Hydroxyethyl)amino)tetrahydrothiophene 1,1-dioxide
https://huagongshe.com/reaction/85712
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiophene, 2,3-dihydro-, 1,1-dioxide | HCID 14497 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-((2-Hydroxyethyl)amino)tetrahydrothiophene 1,1-dioxide | HCID 422971 | — |
Reaction Steps
A mixture of 2-aminoethanol (310 mg, 5.08 mmol), triethylamine (514 mg, 5.08 mmol) and 2,3-dihydrothiophene 1,1-dioxide (200 mg, 1.693 mmol) in ethanol (3 mL) was heated up at 78° C. for 16 hours. TLC indicated the starting material was consumed and desired product was formed (30% methanol/ethyl acetate). The reaction mixture was concentrated under reduced pressure, the residue was purified by silica gel chromatography with 0-35% methanol/ethyl acetate to provide the title compound as a colorless oil (260 mg, 86%). 1H NMR (400 MHz, CHLOROFORM-d) δ 3.78-3.56 (m, 3H), 3.38-3.21 (m, 2H), 3.14-3.00 (m, 1H), 2.94 (dd, J=13.3, 6.0 Hz, 1H), 2.85-2.68 (m, 2H), 2.53-2.34 (m, 1H), 2.22-2.03 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846647B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-13f51c145ffb4e21be9c0353f06a8ebf |
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| Source note | uspto-grants-2014_09 |
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