Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citronellal | HCID 7794 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | 2-Octene, 8,8-dimethoxy-2,6-dimethyl- | HCID 102507 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 13945690 | HCID 13945690 | 85% |
Reaction Steps
A solution of citronellal dimethyl acetal [55.0 g, 275 mmole, prepared from racemic citronellal, according to the process described by V. R. Mamdapur et al. in Tetrahedron 20, 2601 (1964)] in methanol (550 ml) was treated at -75° with a stream of ozone for 3.5 h (4.5 g of O3 per hour, 328 mmole of O3). The excess of ozone was purged with argon, the solution was allowed to warm to 0° and then treated with a solution of NaBH4 (5.22 g, 137.5 mmole) in MeOH-H2O (1:1, 154 ml). After 2 h, the reaction mixture was concentrated at reduced pressure, then extracted with ether, and the organic phase was washed to neutrality, dried over MgSO4 and concentrated at reduced pressure. 60.2 g of the desired hexanol (ca. 85% pure) were thus obtained and this product was used as such in the next preparation step. An analytical sample, obtained by preparative GLC (gas-liquid chromatography) gave the following data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05068362 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-a2171b71e65b472fbfb3c9b741958fcc |
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| Source note | uspto-grants-1991_11 |
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