Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274895Generated: October 31, 2026

(4-Methoxyphenyl)boronic acid → HCID 131733414, compound

https://huagongshe.com/reaction/2274895

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantHCID 68327923HCID 68327923—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 131733414HCID 13173341465%

Reaction Steps

Using general procedure E, quinuclidin-3-yl 1-(4-bromophenyl)cyclopropylcarbamate (0.485 g, 1.33 mmol), 4-methoxyphenyl boronic acid (0.404 g, 2.66 mmol) and Pd(OAc)2 (0.016 g, 0.071 mmol) gave the title compound as a grey solid (0.337 mg, 65%). 1H NMR (CDCl3) δ 7.48 (dd, J=8.6, 5.5 Hz, 4H), 7.29 (d, J=7.6 Hz, 2H), 6.96 (d, J=8.8 Hz, 2H), 5.58 (d, J=48.7 Hz, 1H), 4.83-4.63 (m, 1H), 3.84 (s, 3H), 3.20 (dd, J=24.0, 15.5 Hz, 1H), 2.97-2.42 (m, 5H), 1.97 (d, J=30.9 Hz, 1H), 1.81 (s, 1H), 1.75-1.33 (m, 3H), 1.28 (d, J=6.8 Hz, 4H) ppm. 13C NMR major rotomer (CDCl3) δ 159.1, 156.0, 141.4, 139.0, 133.4, 128.0, 126.7, 125.9, 114.2, 71.5, 55.7, 55.3, 47.4, 46.5, 35.3, 25.5, 24.6, 19.6, 17.8 ppm. Purity: LCMS>97.1% (214 nm & 254 nm); retention time 0.88 min; (M+1) 393.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126993B2
Source datasetuspto-grants-2015_09
ORD IDord-3220cfbc98364fccb8aa1b4326495ca8
Source noteuspto-grants-2015_09