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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794092Generated: November 3, 2026

2,6-Difluorobenzyl alcohol → 2,6-Difluorobenzyl 4-tert-butoxycarbonyl-cis-2,6-dimethylpiperazine-1-carboxylate

https://huagongshe.com/reaction/1794092

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Difluorobenzyl alcoholHCID 87921—
Reactantrel-1,1-Dimethylethyl (3R,5S)-4-(chlorocarbonyl)-3,5-dimethyl-1-piperazinecarboxylateHCID 86585999—
Product2,6-Difluorobenzyl 4-tert-butoxycarbonyl-cis-2,6-dimethylpiperazine-1-carboxylateHCID 69141404—

Reaction Steps

2,6-Difluorobenzyl 4-tert-butoxycarbonyl-cis-2,6-dimethylpiperazine-1-carboxylate was prepared from cis 1-chlorocarbonyl-2,6-dimethyl-4-tert-butoxycarbonylpiperazine and 2,6-difluorobenzyl alcohol according to the method described for Example 54 to give the product as a colourless gum (0.251 g, 65%); Rf (Silica, isopropyl ether) 0.35; δH (400 MHz, CDCl3) 7.29 (1H, m), 6.90 (2H, m), 5.23 (2H, s), 4.16 (2H, m), 3.92 (2H, br), 2.95 (2H, br), 1.47 (9H, s), 1.21 (6H, d, J 6.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022707B2
Source datasetuspto-grants-2006_04
ORD IDord-2aa98fdb3913405eb0b6a50cfcdd272b
Source noteuspto-grants-2006_04