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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582548Generated: October 31, 2026

Sodium Iodide → HCID 10829224, compound

https://huagongshe.com/reaction/582548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantAluminumHCID 5359268—
Reactant5-bromo-1,1-dimethoxypentaneHCID 11074684—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 10829224HCID 1082922463%

Reaction Steps

A mixture of 5-bromovaleraldehyde dimethyl acetal (27.5 g, 0.13 mol), Na2CO3 (20.7 g, 0.195 mol), sodium iodide (19.5 g, 0.13 mol) and tert-butyl-1-piperazinecarboxylate (25.5 g, 0.137 mol), in dimethoxyethane (250 ml), was heated at 100° C. for 3 h. Aluminium foil was wrapped around the vessel to exclude light. The mixture was cooled to room temperature and filtered. The filtrate was evaporated under reduced pressure and then EtOAc (50 ml) added and the mixture filtered again to remove inorganic salts. The solvent was removed under vacuum and the residue chromatographed on silica gel eluting with EtOAc to give the title-product (25.7 g, 63%). δ(250 MHz, CDCl3) 1.29-1.71 (6H, m, 3 of CH2); 1.46 (9H, s, OC(Me)3); 2.31-2.39 (6H, m, 3 of CH2); 3.32 (6H, s, CH(OMe)2); 3.41-3.45 (4H, m, 2 of CH2); 4.36 (1H, t, J=6 Hz, CH(OMe)2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925638
Source datasetuspto-grants-1999_07
ORD IDord-115badc088684a5c9cf14a4f7a688821
Source noteuspto-grants-1999_07