Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 6-Bromo-1-tetralone | HCID 10105069 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 89740081 | HCID 89740081 | 99.9% |
Reaction Steps
6-bromo-3,4-dihydronaphthalen-1(2H)-one (3.5 g, 15.55 mmol), thiourea (3.55 g, 46.6 mmol) and iodine (4.34 g, 17.10 mmol) were dissolved in 20 ml of ethanol and the solution was heated at 100° C. for 4 hr. The volume of ethanol was reduced and the solid amine hydroiodide salt was filtered and washed with ether. The solid obtained was dissolved in water and basified with 10% NaOH solution and extracted with ethyl acetate. The ethyl acetate layer was dried over Na2SO4 and concentrated to obtain the desired compound (4a) (4.37 g, 80%). m/z 280.9 (79Br) & 282.9 (81Br) (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073942B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-5450043ae6db4eefa778df6410f74b12 |
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| Source note | uspto-grants-2015_07 |
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