HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyacetone → 1-Propanol, 2-[(2,3,4-trifluorophenyl)amino]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyacetone | HCID 8299 | — |
| Reactant | 1,2,3-Trifluoro-4-nitrobenzene | HCID 69871 | — |
| Reactant | 2,3,4-Trifluoroaniline | HCID 77468 | — |
| Reactant | 7,8-Difluoro-2,3-dihydro-3-methyl-4H-(1,4)benzoxazine | HCID 10219718 | — |
| Product | 1-Propanol, 2-[(2,3,4-trifluorophenyl)amino]- | HCID 9859097 | — |
Reaction Steps
A method for the preparation of 7,8-difluoro-2,3-dihydro-3-methyl-4H-1,4-benzoxazine either as the optically active s-(-)-7,8-difluoro-2,3-dihydro-3-methyl-4H-1,4-benzoxazine or the racemic mixture. The process of the invention comprises the reaction of 2,3,4-trifluoroaniline or trifluoronitrobenzene with hydroxyacetone or a hydroxyacetone derivative under reducing condition to yield N-(3-hydroxy-2-propyl)-2,3,4-trifluoroaniline derivative. The N-(3-hydroxy-2-propyl)-2,3,4-trifluoroaniline is treated with base to yield the benzoxazine intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05986140 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-ef891973ea5e44ec885fdee9ab3dfaa2 |
| Source note | uspto-grants-1999_11 |