Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 19880012 | HCID 19880012 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54028115 | HCID 54028115 | — |
Reaction Steps
Into 210 ml of dry ether, 10 g of LiAlH4 was added, and under stirring, a solution of the above carboxylic acid in 70 ml of ether was added dropwise in 70 min. while keeping a temperature of 2°-6° C. after the addition, the mixture was raised in temperature to 23° C. and stirred for 3 hours. After standing for 12 hours, 5% hydrochloric acid was added to acidify the mixture while keeping a temperature of below 15° C., and the product was extracted with ether and washed successively with water, 5% NaOH aqueous solution and water, followed by drying with anhydrous MgSO4. By distilling off the solvent and effecting vacuum distillation, 10 g of (S)-4-octyloxypentanol was obtained as a fraction at 150° C./5 mmHg. The product showed the following IR data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05143643 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-316d3b2254304e86ac04238749905f91 |
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| Source note | uspto-grants-1992_09 |
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