HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 15283178, compound → HCID 15283179, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 15283178 | HCID 15283178 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 15283179 | HCID 15283179 | 88.4% |
Reaction Steps
A solution of 0.75 g (2.8 mmoles) 6-nitro-5-ethyl-2-ethoxy-3,1-benzoxazin-4-one in 35 mL ethyl acetate was transferred to a Parr bottle. 0.40 g (0.38 mmoles) of 10% Pd/C catalyst was added. The sample was hydrogenated on a Parr shaker at ambient temperature and 1 atm pressure for 3 hours. The catalyst was removed by filtration through a pad of Celite. The filtrate was concentrated in vacuo to produce a bright yellow solid. There was obtained 0.58 g (86% yield) of 6-amino-5-ethyl-2-ethoxy-3,1-benzoxazin-4-one. NMR(CDCl3): 1.22 (t,3H,J=7.5 Hz), 1.42(t,3H,J=7.2 Hz), 3.14(q,2H,J=7.5 Hz), 4.44(q,2H,J=7.2 Hz), 7.09(d,1H,J=8.7 Hz), 7.14(d,1H,J=8.7 Hz). MS(m/z): 234(M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428021 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-8f12024f2c434531beb141a6d6a8a5aa |
| Source note | uspto-grants-1995_06 |