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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725717Generated: November 1, 2026

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

https://huagongshe.com/reaction/725717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantTetralinHCID 8404—
Reactant5-Iodo-1,2,3,4-tetrahydronaphthaleneHCID 582947—
Reactant6-Iodo-1,2,3,4-tetrahydronaphthaleneHCID 583197—
ReactantHCID 86590690HCID 86590690—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductNaphthalene, 1,2,3,4-tetrahydro-1-iodo-HCID 1132285483.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

132.2 g (1.00 mol) of tetralin was dissolved in 600 ml of 80% acetic acid, and 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 were added thereto. The mixture was heated to 70° C. with stirring. The mixture was further stirred for 3 hours at the same temperature whereupon disappearance of tetralin was confirmed to terminate the reaction. The reaction mixture was added to 1000 ml of water, and the separated oily substance was extracted with 1000 ml of toluene. The toluene layer was washed with water and concentrated and then subjected to distillation under reduced pressure (bp: 120° C./3 mmHg) to obtain 215.3 g of the main fraction (yield: 83.4%). This product was a mixture of 5-iodotetralin and 6-iodotetralin in a blend ratio of 1:2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05707768
Source datasetuspto-grants-1998_01
ORD IDord-4ecffabe8422457b92b95231dc19f407
Source noteuspto-grants-1998_01