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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794118Generated: November 3, 2026

(3-Bromopropyl)benzene → HCID 21021892, compound

https://huagongshe.com/reaction/1794118

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Bromopropyl)benzeneHCID 12503—
Reactant4-Fluoro-3-(hydroxymethyl)phenolHCID 69141614—
Reactantrel-1,1-Dimethylethyl (3R,5S)-4-(chlorocarbonyl)-3,5-dimethyl-1-piperazinecarboxylateHCID 86585999—
ProductHCID 21021892HCID 21021892—

Reaction Steps

2-Fluoro-5-(3-phenyl)propoxybenzyl cis-2,6-dimethylpiperazine-1-carboxylate was prepared from 2-fluoro-5-hydroxybenzyl alcohol, 3-phenylpropyl bromide and 1-chlorocarbonyl-cis-2,6-dimethyl-4-tert-butoxycarbonylpiperazine according to the methods described for Examples 54 and 121 to give the product as a yellow oil (2.3%); HPLC (XTERRA, 50/80, 220 nm) 91.1% (6.29 min); NMR δH (400 MHz, DMSO-d6) 7.32–7.10 (6H, m), 6.95 (1H, q, J 3 Hz), 6.91 (1H, dt, J 9, 4 Hz), 5.08 (2H, s), 3.93 (2H, t, J 6.5 Hz), 3.91 (2H,m), 2.73 (2H, t, J 7 Hz), 2.71 (2H, d, J 8.5 Hz), 2.65 (2H, dd, J 12.5, 4.5 Hz), 2.00 (2H, m) and 1.18 (6H, d, J 7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022707B2
Source datasetuspto-grants-2006_04
ORD IDord-68dcfc5b7d3d418d913b70dc4c8121a3
Source noteuspto-grants-2006_04