Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274906Generated: October 31, 2026

Phenylboronic Acid → HCID 68327951, compound

https://huagongshe.com/reaction/2274906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 68328080HCID 68328080—
ProductHCID 68327951HCID 6832795147%

Reaction Steps

Using general procedure E, quinuclidin-3-yl 3-bromobenzylcarbamate (237 mg, 0.700 mmol), phenylboronic acid (171 mg, 1.4 mmol) and [PdCl2(pddf)]CH2Cl2 gave the title compound as a viscous semi-solid (110 mg, 47%). 1H NMR (500 MHz, CDCl3) δ 7.57 (d, J=7.5 Hz, 2H), 7.50 (m, 2H), 7.62-7.38 (m, 3H), 7.35 (t, J=7.5 Hz, 1H), 7.28 (d, J=8.0 Hz, 1H), 5.32-5.17 (m, 1H), 7.78 (m, 1H), 4.42 (d, J=6.0 Hz, 2H), 3.26 (m, 1H), 2.95-2.65 (m, 5H), 2.05 (m, 1H), 1.84 (m, 1H), 1.70 (m, 1H), 1.58 (m, 1H), 1.42 (m, 1H) ppm. 13C NMR (125 MHz, CDCl3) δ 155.2, 140.7, 139.8, 138.0, 128.1, 127.8, 126.4, 126.1, 125.5, 125.4, 125.3, 70.1, 54.4, 46.2, 45.3, 44.1, 24.3, 23.1, 18.2 ppm. Purity: >98% LCMS (214 nm & 254 nm); retention time 1.44 min; (M+1) 337.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126993B2
Source datasetuspto-grants-2015_09
ORD IDord-5e591bb3b76847088f38de3300caaf3c
Source noteuspto-grants-2015_09