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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516944Generated: October 25, 2026

Sulfuric Acid → 6-iodo-3,4-dihydronaphthalen-1(2H)-one

https://huagongshe.com/reaction/516944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium IodideHCID 5238—
Reactant6-Amino-1,2,3,4-tetrahydronaphthalen-1-oneHCID 339537—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product6-iodo-3,4-dihydronaphthalen-1(2H)-oneHCID 4548980068.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred clear solution of 6-amino-3,4-dihydronaphthalen-1(2H)-one (15 g, 93 mmol) in acetic acid (150 mL) and water (150 mL) was added sulfuric acid (5.5 mL, 101 mmol) dropwise at 0° C. A solution of sodium nitrite (12.90 g, 187 mmol) in water (100 mL) was then added dropwise over 40 min at the same temperature. The mixture was stirred at 0° C. for 10 min before being added to a stirred solution of sodium iodide (55.8 g, 372 mmol) in water (600 mL) slowly over 2 h at 0° C. The resulting brown suspension was stirred at 0° C. for 30 min and at room temperature for 1 h. The mixture was extracted with ethyl acetate (400 mL, 2×100 mL). The combined ethyl acetate extracts were washed with water (60 mL), saturated aqueous Na2S2O3 solution until the brown color disappeared, and saturated aqueous K3PO4 (60 mL) solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Flash chromatography purification (330 g silica gel column, gradient elution from 5 to 15% ethyl acetate in hexanes) afforded 6-iodo-3,4-dihydronaphthalen-1(2H)-one (17.3 g, 63.6 mmol) as a solid. LC/MS M+1=273.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115054B2
Source datasetuspto-grants-2015_08
ORD IDord-c3c5a9c3e236430abd695b0db7c1139a
Source noteuspto-grants-2015_08