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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447320Generated: October 26, 2026

p-Diiodobenzene → (R)-1-(4-iodophenyl)-N,N-dimethylpyrrolidin-3-amine

https://huagongshe.com/reaction/447320

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-DiiodobenzeneHCID 12208—
Reactant(3R)-(+)-3-(Dimethylamino)pyrrolidineHCID 2758521—
Reactant1-(4-Bromophenyl)-cis-3,5-dimethylpiperazineHCID 66730361—
Product(R)-1-(4-iodophenyl)-N,N-dimethylpyrrolidin-3-amineHCID 66730449—

Reaction Steps

The title compound was synthesized according to the synthesis of 1-(4-bromophenyl)-cis-3,5-dimethylpiperazine, except reacting 1,4-diiodobenzene (2.41 g, 7.30 mmol) with (R)—N,N-dimethylpyrrolidin-3-amine (1.0 g, 8.8 mmol). The title compound was purified by silica gel chromatography (MeOH/CH2Cl2, 2:98 to 12:88) as a yellow solid (1.17 g, 51%). 1H NMR (400 MHz, MeOD) δ 7.42 (d, J=8.2 Hz, 2H), 6.39 (d, J=8.0 Hz, 2H), 3.51-3.47 (m, 1H), 3.44-3.39 (m, 1H), 3.29-3.24 (m, 1H), 3.13-3.09 (m, 2H), 3.00-2.87 (m, 1H), 2.35 (s, 6H), 2.35-2.26 (m, 1H), 1.96-1.86 (m, 1H); MS ESI 317.0 [M+H]+, calcd for [C12H17IN2+H]+ 317.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481533B2
Source datasetuspto-grants-2013_07
ORD IDord-57b08ec44a534953acdd55626e34bd64
Source noteuspto-grants-2013_07