HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979512Generated: October 31, 2026
Hydrogen Bromide → 1-(1,2,3,4-Tetrahydro-4,4-dimethyl-1-naphthalenyl)-1-propanone
https://huagongshe.com/reaction/1979512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | HCID 20439314 | HCID 20439314 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(1,2,3,4-Tetrahydro-4,4-dimethyl-1-naphthalenyl)-1-propanone | HCID 166445 | 24% |
Reaction Steps
In a 3-liter flask provided with a thermometer and stirrer 200 g of phosphorus pentoxide are added while cooling to 500 g of 85% phosphoric acid and subsequently 150 g of 4-cyano-7-methyl-4-phenyl-oct-6-en-3-one are added at ca. 50° C. The mixture is stirred at 105° C. until starting material is no longer present (gas chromatography/thin-layer). 1000 g of 48% hydrobromic acid and 500 g of glacial acetic acid are then added. After 12 hours, a further 200 g of 48% hydrobromic acid and 100 g of glacial acetic acid are added and the temperature is raised to 110° C. After a total reaction time of 30 hours, the mixture is cooled, ice is added and the mixture is extracted with ether, washed neutral with water, with 10% sodium hydroxide and again with water, dried over sodium sulphate and evaporated. Vacuum distillation gives 32 g of 1,1-dimethyl-4-propionyl-tetralin of boiling point 75° C./0.05 mmHg; nD20 =1.5263; yield 24%. Odour: see (3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04481133 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-af7bdc69fc9c44fd9049e65d8bfd7f6c |
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| Source note | uspto-grants-1984_11 |
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