HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Methoxy-3,7-Dimethyloctanal → 1-Octanol, 7-methoxy-3,7-dimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Methoxy-3,7-Dimethyloctanal | HCID 19223 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Octanol, 7-methoxy-3,7-dimethyl- | HCID 170041 | — |
Reaction Steps
93.2 g. of 7-methoxycitronellal dissolved in 200 ml. of absolute diethyl ether are added dropwise with ice cooling to a suspension of 7.6 g. of lithium aluminum hydride in 500 ml. of absolute diethyl ether. Subsequently, the mixture is stirred for 30 minutes and decomposed in the cold by the addition of 100 ml. of aqueous ammonium chloride solution. The resulting mass is filtered through diatomaceous earth, the filtrate washed once with saturated aqueous ammonium chloride solution and once with saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. The residue is distilled at 0.1 mmHg. There is obtained pure 3,7-dimethyl-7-methoxy-1-octanol of boiling point 87° C./0.1 mmHg; nD20 = 1.4456.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002647 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-a77c08cb12cc4c3ea5c1504bb4eb23e0 |
| Source note | uspto-grants-1977_01 |