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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537977Generated: October 31, 2026

Hydrochloric Acid → 6-Iodoindane-5-carbaldehyde

https://huagongshe.com/reaction/537977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantDiethyl EtherHCID 3283—
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant6-Iodoindane-5-carbonitrileHCID 57576269—
SolventDichloromethaneHCID 6344—
Product6-Iodoindane-5-carbaldehydeHCID 8662614573%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 6-iodoindane-5-carbonitrile (36.5 mg, 0.136 mmol) in dichloromethane (1.0 mL) under N2 at −78° C. was added a solution of 1N DIBALH in toluene (272 μL, 0.272 mmol) dropwise. The reaction was stirred at −78° C. for 15 min. Keeping the temperature at −78° C., another two portions of DIBALH (100 μL each) were added until the starting material disappeared by TLC. The reaction mixture was poured into 2N HCl (45 mL) and diluted with Et2O. The mixture was stirred for 0.5 h. The Et2O layer was separated. The aqueous layer was extracted with Et2O (2×). The organic extracts were combined, dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography (Si, hexanes/EtOAc) to afford 6-iodoindane-5-carbaldehyde (27 mg, 73%). 1H NMR (500 MHz, CDCl3) δ 10.08 (s, 1H), 7.83 (s, 1H), 7.79 (s, 1H), 2.98 (t, J=7.5 Hz, 2H), 2.94 (t, J=7.5 Hz, 2H,), 2.19-2.13 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865707B2
Source datasetuspto-grants-2014_10
ORD IDord-ef0778e71f4b412a90a9aa86fa742a19
Source noteuspto-grants-2014_10