HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 68325563, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Tetrahydrofuran ethyl acetate | HCID 21939870 | — |
| Reactant | HCID 86671405 | HCID 86671405 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68325563 | HCID 68325563 | — |
Reaction Steps
To a stirred solution of (RS)-2-(4-bromo-3-chloro-phenyl)-oxirane (15.2 g) in THF (40 ml) was added 2-aminoethanol (35.1 ml) and the mixture was stirred at room temperature for 7 hours. The reaction mixture was then poured into EtOAc/THF (1:1) and washed with saturated brine. The organic layer was separated and was then dried over Na2SO4 and concentrated in vacuo to afford (RS)-1-(4-bromo-3-chlorophenyl)-2-(2-hydroxyethylamino)ethanol (19.0 g) as a yellow oil which was used in the next step without further purification. MS (ISP): 298.1 ([{81Br37Cl}M+H]+), 296.0 ([{81Br35Cl or 79Br37Cl}M+H]+), 293.9 ([{79Br35Cl}M+H]).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802673B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-b7b5f73edcb546c5ab9b5716e8f22815 |
| Source note | uspto-grants-2014_08 |