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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380189Generated: October 30, 2026

Potassium Iodide → 9,9-Diethyl-7-iodofluorene-2-carboxaldehyde

https://huagongshe.com/reaction/380189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDimethylformamideHCID 6228—
ReactantTributylphosphineHCID 13831—
Reactant7-Bromo-9,9-diethylfluorene-2-carboxaldehydeHCID 15476349—
CatalystNickel(II) bromideHCID 278492—
SolventTolueneHCID 1140—
Product9,9-Diethyl-7-iodofluorene-2-carboxaldehydeHCID 1836892175%

Reaction Steps

A mixture of 9,9-diethyl-7-bromofluorene-2-carboxaldehyde, (28.8 g., 0.0875 mol.), nickel (II) bromide (2.1 g., 9.6 mmol.), tri-n-butyl phosphine (4m1, 16 mmol.), potassium iodide (52.0 g., 0.3132 mole, 3.6 equivalents), and DMF (125 ml), was held at reflux under an atmosphere of nitrogen for 15 hours, cooled, diluted with toluene (450 ml), and filtered. The filtrate was washed with water in several portions, dried, and concentrated. The residual solids were recrystallized from toluene-heptane (1:2, 150 ml); 24.79 g., m.p. 138-140° C., (75% yield). When the reaction was run longer, 24 and 34 hours, the yields fell to 61 and 59% respectively. Mass Spec (m/z): 376 (M+), not contaminated with the bromo aldehyde. Anal.Calcd. for C18H17Ol: C, 57.46; H, 4.55; and l, 33.73%. Found: C, 58.04 and 58.02; H, 4.72 and 4.66; and l, 32.62 and 32.89.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300502B1
Source datasetuspto-grants-2001_10
ORD IDord-3d180c16ac664feaa26e72325d6d731b
Source noteuspto-grants-2001_10