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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277004Generated: October 30, 2026

3-Nitrophenylboronic Acid → HCID 178418989, compound

https://huagongshe.com/reaction/277004

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
ReactantHCID 178419047HCID 178419047—
ProductHCID 178418989HCID 17841898955%

Reaction Steps

Prepared from 5′-bromospiro{cyclohexane-1,3′-[3H]indol}-2′(1′H)-one 2′(O-benzyloxime) (1.0 g, 2.6 mmol) and 3-Nitrophenyl boronic acid (0.86 g, 5.2 mmol) according to Example 45 procedure A. Purification by flash silica gel chromatography (eluant: 10:0.5 hexane:ethyl acetate) afforded the desired compound (0.60 g, 1.4 mmol, 55%) as a viscous oil. 1H NMR (500 MHz, DMSO-d6) δ 1.42-1.82 (8H, m) 2.02-2.04 (2H, q) 5.01 (2H, s) 6.88 (1H, d) 7.28-7.71 (8H, m) 8.08-8.13 (2H, m) 8.38 (1H, d) 9.69 (1H, s); MS (ESI(−ve)) m/z 426 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355648B1
Source datasetuspto-grants-2002_03
ORD IDord-f2a3a4bcc6ca457cad9c1516c6882264
Source noteuspto-grants-2002_03