HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 68325669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Tetrahydrofuran ethyl acetate | HCID 21939870 | — |
| Reactant | HCID 86671392 | HCID 86671392 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68325669 | HCID 68325669 | — |
Reaction Steps
To a stirred solution of (RS)-2-(3-methyl-4-nitrophenyl)oxirane (4.63 g) in THF (15 ml) was added 2-aminoethanol (15.5 ml) and the mixture was stirred at room temperature overnight. The reaction mixture was then poured into EtOAc/THF (1:1) and extracted with saturated brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to afford (RS)-2-(2-hydroxyethylamino)-1-(3-methyl-4-nitrophenyl)ethanol (6.84 g, quant.) as a brown oil which was used in the next step without further purification. MS (ISP): 241.1 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802673B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-77b5de7ebb884e2a953ee46237315712 |
| Source note | uspto-grants-2014_08 |