HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357702Generated: October 29, 2026
Iodine → Naphthalene, 1,2,3,4-tetrahydro-1-iodo-
https://huagongshe.com/reaction/357702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Tetralin | HCID 8404 | — |
| Reactant | 1-Iodo-5,6,7,8-tetrahydronaphthalene | HCID 582947 | — |
| Reactant | 6-Iodo-1,2,3,4-tetrahydronaphthalene | HCID 583197 | — |
| Reactant | HCID 86590690 | HCID 86590690 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Naphthalene, 1,2,3,4-tetrahydro-1-iodo- | HCID 11322854 | 83.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05840980 |
|---|
| Source dataset | uspto-grants-1998_11 |
|---|
| ORD ID | ord-a851ea0fabdd4697a3703234a0f21136 |
|---|
| Source note | uspto-grants-1998_11 |
|---|