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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589059Generated: October 27, 2026

Benzene--cyclohexane (1/1) → 3-ethyl-5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/589059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene--cyclohexane (1/1)HCID 18624872—
Reactant5-nitro-3-pyridin-2-yl-2H-1,4-benzoxazineHCID 90408902—
ReactantHCID 178506846HCID 178506846—
SolventTetrahydrofuranHCID 8028—
Product3-ethyl-5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazineHCID 90409367—

Reaction Conditions

Temperature-78 °C

Reaction Steps

0.5 M Ethyl lithium in benzene-cyclohexane (1.8 mL, 0.88 mmol) was added drop-wise to a solution of 5-nitro-3-pyridin-2-yl-2H-1,4-benzoxazine (0.025 g, 0.88 mmol) in tetrahydrofuran (4 mL), cooled to −78° C. The reaction was stirred for 1 h at −78° C. and was then quenched with methanol. The reaction mixture was partitioned between ethyl acetate and water, and the organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated to give crude product. The product was purified by FCC on silica gel eluting a hexane:ethyl acetate gradient to give 3-ethyl-5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazine as a solid (0.021 g. 84%). LCMS calculated for C15H16N3O3 (M+H)+: m/z=286.1. found: 286.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227985B2
Source datasetuspto-grants-2016_01
ORD IDord-201ae97b463f4655806c488d4a39f5b9
Source noteuspto-grants-2016_01