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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228465Generated: October 30, 2026

Potassium Iodide → HCID 18469926, compound

https://huagongshe.com/reaction/2228465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-MethylhomopiperazineHCID 228349—
ReactantHCID 18469942HCID 18469942—
SolventDimethylformamideHCID 6228—
ProductHCID 18469926HCID 18469926—

Reaction Steps

N-Methylhomopiperazine (2.31 g; 20.2 mmol) and potassium iodide (0.35 g; 2.2 mmol) in DMF (13 ml) were reacted with 1-chloro-6-bromo-1,2,3,4-tetrahydronapthalene (2.48 g; 10.1 mmol) in DMF (8 ml) as in Example 15. The yellow oil was kugelrohr distilled to give the title compound, 1.47 g, bp (air bath temperature) 152°-165° C. at 0.10 torr; 1H NMR (300 MHz, CDCl3) δ 2.38 (s, 3H, NCH3), 3.81 (t, 1H, ArCHN), 7.19 (s, 1H), 7.25 (d, 1H), 7.64 (d, 1H). Anal: Calcd. for C16H23BrN2: C, 59.45; H, 7.17; N, 8.67. Found: C, 59.40; H, 7.02; N, 8.30. 1-Chloro-6-bromo-1,2,3,4-tetrahydronaphthalene was prepared as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417183B1
Source datasetuspto-grants-2002_07
ORD IDord-92d17fd6d6714d569ac46cd7d108cf03
Source noteuspto-grants-2002_07