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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593008Generated: November 3, 2026

4-(Methylsulfonyl)benzyl Bromide → HCID 58797590, compound

https://huagongshe.com/reaction/1593008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methylsulfonyl)benzyl BromideHCID 2733581—
ReactantTert-butyl 4-(2H-tetrazol-5-YL)piperidine-1-carboxylateHCID 18187701—
ReactantHCID 58797593HCID 58797593—
ProductHCID 58797590HCID 58797590—

Reaction Steps

This was prepared from 4-methanesulphonylbenzyl bromide and tert-butyl 4-(2H-tetrazol-5-yl)piperidine-1-carboxylate using a similar method to that used to prepare 4-[2-(4-chloro-benzyl)-2H-tetrazol-5-yl]-piperidine (Method G, Steps 4 and 5); NMR (CDCl3): 1.8 (m, 2H), 2.05 (m, 2H), 2.8 (m, 2H), 3.05 (s, 3H), 3.1 (m, 1H), 3.2 (m, 2H), 5.89 (s, 2H), 7.55 (d, 2H), 7.95 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294636B2
Source datasetuspto-grants-2007_11
ORD IDord-87564830a2fd431892235545d6e9fa6f
Source noteuspto-grants-2007_11