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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9335Generated: October 26, 2026

3-Nitrophenylboronic Acid → HCID 178418989, compound

https://huagongshe.com/reaction/9335

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 numberUS07091234B2
Source datasetuspto-grants-2006_08
ORD IDord-0339de4b5b6c487c862e7caab6206f02
Source noteuspto-grants-2006_08