Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 20474311 | HCID 20474311 | — |
| Product | HCID 53831434 | HCID 53831434 | — |
Reaction Steps
To 10.9 g. of potassium hydroxide of the same grade used in the examples above was added 50 ml. of butanol, and the mixture was stirred for 1 hour. To it was added 5.0 g. of 1,1,1-trichloro-2-(3-chloro-2-methylphenyl)ethane, and the mixture was stirred under reflux at 115° for 6 hours and allowed to cool overnight to ambient temperature. The mixture was then worked up as described in Example 4 above to obtain 4.5 g. of crude product as the major product. It was then taken up in 15 ml. of butanol and stirred with 40 ml. of 1 N hydrochloric acid at ambient temperature for 30 minutes. The layers were then separated, extracted and dried as described in Example 5 above to obtain 3.41 g. of product, found to be 92% pure by vapor phase chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04426536 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-127d98232a1948bf9b1c07d304e4b5c1 |
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| Source note | uspto-grants-1984_01 |
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