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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265432Generated: October 27, 2026

Potassium Iodide → 7-iodo-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one

https://huagongshe.com/reaction/265432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant7-Amino-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-oneHCID 15462841—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product7-iodo-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-oneHCID 11415342—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4,4-dimethyl-7-amino-1-tetralone (XII) (1.82 g, 10.0 mmol) in concentrated hydrochloric acid (4.69 mL) was added ice cold water (3.13 mL). The reaction mixture was then cooled to 0° C. by use of an ice-salt bath. The reaction mixture was then diazotized by the dropwise addition with stirring of a solution of sodium nitrite (0.76 g, 11.0 mmol) in water (3.13 mL) keeping temperature between 0°-5° C. After stirring for 15 minutes, the reaction mixture was added to a solution of potassium iodide (3.63 g, 21.9 mmol) in water (18.8 mL). After standing for 30 minutes, the dark gum was extracted with ethyl acetate (1×100 mL). The organic phase was then concentrated in vacuo and the residue chromatographed on silica gel (eluted with 5% ethyl acetate in hexane) to give 1.56 g (Y: 54%) of the title product; 1H-NMR (CDCl3): δ 8.33 (d, J=2.0 Hz, 1H), 7.82 (dd, J=8.3, 2.0 Hz, 1H), 7.17 (d, J=8.4 Hz, 1H), 2.72 (t, J=6.8 Hz, 2H), 2.01 (t, J=6.8 Hz, 2H), 1.37 (s, 6H); MS (DCI) m/e: 301 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648385
Source datasetuspto-grants-1997_07
ORD IDord-d4b7de97ee0f4120a43dae45a43d4f99
Source noteuspto-grants-1997_07