Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloral | HCID 6407 | — |
| Reactant | 2-Ethylhexanol | HCID 7720 | — |
| Catalyst | HCID 131719147 | HCID 131719147 | — |
| Solvent | 2,2,4-Trimethylpentane | HCID 10907 | — |
| Product | HCID 13783049 | HCID 13783049 | — |
Reaction Steps
In a separate reaction vessel, the chloral 2-ethylhexyl hemiacetal was prepared from 1.05 g 2-ethyl-1-hexanol and 1.19 g (0.00807 mole) chloral substantially as described in Example 3. This material was dispersed in 1 ml of iso-octane and was added dropwise over twenty minutes to the 3,5-dimethylanisole/iso-octane/TiCl4 mixture. A sticky material precipitated, but the reaction solution was stirred at -15° C. for 4.5 hours before being with quenched with water, treated with NaOH, and worked-up substantially as described in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05457239 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-3c0b3873e4a7432ca8e9373327eb4e0d |
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| Source note | uspto-grants-1995_10 |
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