Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794129Generated: October 31, 2026

3-Fluorobenzyl bromide → HCID 69141024, compound

https://huagongshe.com/reaction/1794129

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorobenzyl bromideHCID 68007—
Reactant4-Fluoro-3-(hydroxymethyl)phenolHCID 69141614—
Reactantrel-1,1-Dimethylethyl (3R,5S)-4-(chlorocarbonyl)-3,5-dimethyl-1-piperazinecarboxylateHCID 86585999—
ProductHCID 69141024HCID 69141024—

Reaction Steps

2-Fluoro-5-(3-fluorobenzyl)oxybenzyl cis-2,6-dimethylpiperazine-1-carboxylate was prepared from 2-fluoro-5-hydroxybenzyl alcohol, 3-fluorobenzyl bromide and 1-chlorocarbonyl-cis-2,6-dimethyl-4-tert-butoxycarbonylpiperazine according to the procedures described for Examples 121 and 54 to give the product as a yellow oil: δH (400 MHz, DMSO-d6) 1.28 (6H, d, J 6.9 Hz), 2.77–2.90 (4H, m), 4.10 (2H, br), 5.03 (2H, s), 5.17 (2H, s), 6.85 (1H, m), 6.95–7.10 (3H, m), 7.15 (2H, m) and 7.35 (1H, m), NH not observed; HPLC (XTERRA, 50/80%, 220 nm) 85% (4.83 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022707B2
Source datasetuspto-grants-2006_04
ORD IDord-32ceb663e44440cc99342f079fb711fb
Source noteuspto-grants-2006_04