HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylethanolamine → HCID 178474919, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylethanolamine | HCID 8880 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 178527054 | HCID 178527054 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178474919 | HCID 178474919 | 29.7% |
Reaction Steps
To a solution of 0.31 g (1.5 mmol) of 1,3-dicyclohexylcarbodiimide in tetrahydrofuran (3 ml) is added 0.28 g (1.5 mmol) of 3-phenylpropylphosphinic acid in tetrahydrofuran (1 ml). The resulting suspension is stirred for 10 minutes at room temperature. N-acetyl ethanolamine (0.10 g, 1.0 mol) is then added, followed by 18 mg or 4-dimethylaminopyridine. The mixture is stirred for 2 hours. The solvent is evaporated under reduced pressure, and the residue is stirred with ethyl acetate (20 ml). The resulting suspension is filtered. The filtrate is washed with 5% potassium hydrogen sulfate (8 ml), saturated sodium bicarbonate (2×5 ml), and brine (5 ml), and evaporated to give 0.12 g of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05189023 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-e097ebdedb164acfaf46a0b775e3c606 |
| Source note | uspto-grants-1993_02 |