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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794083Generated: November 2, 2026

Benzyl Alcohol → Benzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride

https://huagongshe.com/reaction/1794083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactantrel-1,1-Dimethylethyl (3R,5S)-4-(chlorocarbonyl)-3,5-dimethyl-1-piperazinecarboxylateHCID 86585999—
ProductBenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochlorideHCID 69142638—

Reaction Steps

Benzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride was prepared from cis 1-chlorocarbonyl-2,6-dimethyl-4-tert-butoxycarbonylpiperazine and benzyl alcohol according to the methods described for Examples 52 and 54 to give the product as a cream solid (0.0833 g, 15% overall); νmax (nujol)/cm−1 2776, 2672, 2568, 2527, 1706, 1581, 1415, and 1329; δH (400 MHz, DMSO-d6) 9.89 (1 H, br), 9.19 (1 H, br), 7.41–7.31 (5H, m), 5.13 (2 H, s), 4.34 (2 H, m), 3.17–3.08 (4 H, m), and 1.31 (6 H, d, J 7.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022707B2
Source datasetuspto-grants-2006_04
ORD IDord-401117db35a74fc4b616d2c73a785576
Source noteuspto-grants-2006_04