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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256504Generated: October 29, 2026

Iodine → Naphthalene, 1,2,3,4-tetrahydro-1-iodo-

https://huagongshe.com/reaction/2256504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantTetralinHCID 8404—
Reactant1-Iodo-5,6,7,8-tetrahydronaphthaleneHCID 582947—
Reactant6-Iodo-1,2,3,4-tetrahydronaphthaleneHCID 583197—
ReactantHCID 86590690HCID 86590690—
SolventAcetic AcidHCID 176—
ProductNaphthalene, 1,2,3,4-tetrahydro-1-iodo-HCID 1132285483.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

In 600 ml of 80% acetic acid was dissolved 132.2 g (1.00 mol) of tetralin. To this solution were added 101.5 g (0.40 mol) of iodine, 45.5 g (0.20 mol) of periodic acid dihydrate, and 15 ml of concentrated sulfuric acid. This mixture was heated to 70° C. with stirring and then stirred at this temperature for 3 hours. After disappearance of the tetralin was ascertained, the reaction was terminated. The reaction mixture was added to 1,000 ml of water, and the oily matter separated was extracted with 1,000 ml of toluene. The toluene layer was washed with water, concentrated, and then distilled at a reduced pressure (boiling point: 120° C./3 mmHg). As a result, the main fraction was obtained in an amount of 215.3 g (yield; 83.4%). This reaction product was a 1:2 mixture of 5-iodotetralin and 6-iodotetralin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654481
Source datasetuspto-grants-1997_08
ORD IDord-e445c27a4fbf4c5781a95de24b8d7fc7
Source noteuspto-grants-1997_08