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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243235Generated: October 29, 2026

(R)-8-Fluoro-3-methyl-5-nitro-3,4-dihydro-2H-benzo[1,4]oxazine → (R)-8-Fluoro-3-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-5-ylamine

https://huagongshe.com/reaction/243235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-8-Fluoro-3-methyl-5-nitro-3,4-dihydro-2H-benzo[1,4]oxazineHCID 68157836—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(R)-8-Fluoro-3-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-5-ylamineHCID 68158450103.4%

Reaction Steps

A suspension of (R)-8-fluoro-3-methyl-5-nitro-3,4-dihydro-2H-benzo[1,4]oxazine (183 mg, 0.86 mmol) and 10% Pd/C (37 mg) in EtOAc (12 mL) and IMS (1.2 mL) was stirred under a H2 balloon for 16 h. The reaction mixture was filtered through celite and the filtrate was concentrated in vacuo to give the title compound as a pale yellow oil (162 mg, quant.). 1H NMR (CDCl3, 300 MHz): δ 6.36 (1H, dd, J=10.6, 8.6 Hz), 6.14 (1H, dd, J=8.6, 4.6 Hz), 4.19 (1H, dd, J=10.4, 2.7 Hz), 3.65 (1H, dd, J=10.4, 8.0 Hz), 3.44 (1H, dqd, J=8.0, 6.5, 2.7 Hz), 3.13 (3H, br s), 1.17 (3H, d, J=6.5 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-c555ed462a75415f97aab36c0e48f0bd
Source noteuspto-grants-2014_02