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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631869Generated: November 2, 2026

Allyl bromide → Benzenemethanamine, N-(2-iodophenyl)-

https://huagongshe.com/reaction/1631869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant2-IodoanilineHCID 11995—
ReactantCesium hydroxideHCID 62750—
SolventDimethylformamideHCID 6228—
ProductBenzenemethanamine, N-(2-iodophenyl)-HCID 10040964—

Reaction Steps

N-benzyl-2-iodoaniline was prepared using a system (FRX 200, Syrris Limited) including a microflow reactor. For this purpose, 329 mg (1.5 mmol) of 2-iodoaniline and 15 ml of dimethylformamide were added to the first storage unit of the system including the microflow reactor to dissolve the 2-iodoaniline, and then 112 mg (0.75 mmol) of cesium hydroxide was added thereto. Meanwhile, 156 μl (1.8 mmol) of allyl bromide and 15 ml of dimethylformamide were added to the second storage unit of the system, and then 112 mg (0.75 mmol) of cesium hydroxide was added thereto. The reactants included in the first and second storage units were transferred through the first and second flow channels to the mixing unit, and then transferred to the microflow reactor including microchannels through the third flow channel. The first and second flow channels could transfer 5 ml (2.5 ml for each flow channel) of the reactants to the microflow reactor. The microflow reactor was set at a capacity of 1 ml, a temperature of 236° C. and a pressure of 7 bar. The reactants in the first and second reactants were set such that they were passed through the first to third flow channels at a flow rate of 0.4 ml/min and introduced into the microflow reactor. Also, the residence time of the reactants in the microflow reactor was set to 2.5 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791301B2
Source datasetuspto-grants-2014_07
ORD IDord-7ee1a37dc97c4b959f938e21f42ea497
Source noteuspto-grants-2014_07