HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660571Generated: October 31, 2026
Dihydro-alpha-ionone → HCID 20531507, compound
https://huagongshe.com/reaction/1660571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dihydro-alpha-ionone | HCID 35821 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20531507 | HCID 20531507 | 34.3% |
Reaction Steps
A solution of sodium bromide (6.17 g) in water (10 ml) and commercial bleach (31.2 ml of a solution of sodium hypochlorite) were stirred together for 5 minutes and a solution of dihydro-α-ionone (3.88 g) in methylene chloride was added. Then a solution of potassium phosphate (monobasic) (5.44 g) in water (30 ml) was added during 30 minutes. After stirring for 50 minutes at 25° a solution of sodium bromide (2.05 g) and commercial bleach (10 ml) was added, followed by a solution of potassium phosphate (monobasic) (2.72 g) in water (10 ml) and the reaction mixture stirred for 15 minutes at 25°. The methylene chloride solution was washed with sodium bicarbonate solution and the solvent evaporated to provide the crude product (5.86 g). Column chromatography gave 1.87 g of 4-(5-bromo-6-methylene-2,2-dimethylcyclohexyl)-2-butanone. NMR (CDCl3) δ0.93 (6H, s, >C(CH3)2), 0.9-2.6 (9H, m), 2.12 (3H, s, --COCH3), 4.6-5.1 (1H, m, >CHBr), 4.76 and 5.28 (2H, 2s, >C=CH2), 4.68 and 5.20 (2H, 2s, >C=CH2, minor isomer; isomer ratio 3/1). IR (film) νmax 2960, 1720, 1675, 1650, 1455, 1360.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04308401 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-44aaad8b1487466e9e846d86f18c8b3b |
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| Source note | uspto-grants-1981_12 |
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