Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-Chloropropane | HCID 6361 | — |
| Reactant | 3,5-Dimethylhexanal | HCID 89226 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22990510 | HCID 22990510 | 70.5% |
Reaction Steps
26.4 g (1.1 gram atom) of magnesium shavings and 100 ml of dry ether are added to a round flask which is provided with a stirrer, condenser, thermometer and dropping funnel. There is now slowly added thereto a solution of 86.4 g (1.1 mol) of isopropyl chloride in 150 ml of anhydrous ether and the mixture is held at reflux temperature. The reaction is initiated by the addition of a small amount of iodine to the magnesium. After completion of the addition of the isopropyl chloride, the mixture is held for a further 1 hour at reflux temperature. There are now slowly added thereto at 5° C. 128.2 g (1 mol) of 3,5-dimethylhexanal dissolved in 250 ml of anhydrous ether. The mixture is again held for 3 hours at reflux temperature. The mixture is then cooled down to 0° C. and the product is decomposed by the addition of 340 ml of ice-cold 10% hydrochloric acid. The ethereal solution is washed neutral with water and dried, and the solvent is evaporated. There are thus obtained 176 g (70%) of crude product, fractional distillation of which yields 121.4 g of 2,5,7-trimethyl-octan-3-ol of boiling point 79° C./5 mmHg; nD20 =1.4362.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04198532 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-e4e064ad112947b9af98d516d4609561 |
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| Source note | uspto-grants-1980_04 |
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