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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413133Generated: October 28, 2026

3-Nitrophenylboronic Acid → 6(3-Nitrophenyl)-spiro[4H-3,1-benzoxazine-4,1'-cyclohexane]-2(1H)-one

https://huagongshe.com/reaction/413133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
Reactant6-Bromospiro[4H-3,1-benzoxazine-4,1'-cyclohexan]-2(1H)-oneHCID 22021904—
Product6(3-Nitrophenyl)-spiro[4H-3,1-benzoxazine-4,1'-cyclohexane]-2(1H)-oneHCID 9923921—

Reaction Steps

Prepared from 6-bromo-spiro[4H-3,1-benzoxazine-4,1′-cyclohexane]-2(1H)-one and 3-nitrophenyl boronic acid according to Procedure A. Off-white solid: mp 245-246° C. 1H-NMR (CDCl3) δ8.39 (t, 1H, J=1.9 Hz), 8.20 (dd, 1H, J=8.2, 1.4 Hz), 8.11 (s, 1H, D2O exchangeable), 7.86 (d, 1H, J=8.0 Hz), 7.62 (t, 1H, J=8.1 Hz), 7.50 (dd, 1H, J=8.2, 1.9 Hz), 7.39 (d, 1H, J=1.8 Hz), 6.93 (d, 1H, J=8.2 Hz), 2.25 (d, 2H, J=12.7 Hz), 1.60-1.99 (m, 7H), 1.31-1.42 (m, 1H); MS (EI) m/z 337 ([M−H]−, 100%). Anal. Calc. For C19H18N2O4.0.35H2O: C, 66.21, H, 5.47, N, 8.13. Found: C, 66.22, H, 5.43, N, 7.86.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566358B2
Source datasetuspto-grants-2003_05
ORD IDord-7c1e82afda0344778e9745b6af154d36
Source noteuspto-grants-2003_05