Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromohexadecane | HCID 8213 | — |
| Reactant | 2,4-Dichloro-5-hydroxyacetanilide | HCID 2735988 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 22753009 | HCID 22753009 | 74.8% |
Reaction Steps
In a solution of 5.6 g of potassium hydroxide in 200 ml of ethanol was dissolved 22 g of 4,6-dichloro-3-acetaminophenol (which was synthesized using the method described in Beilstein, 13, I, 135). To the solution was added 30.5 g of hexadecyl bromide. After the mixture was stirred for an hour at room temperature (about 20-30° C.), the mixture was heated at reflux for 8 hours. The reaction mixture was poured into water. The resulting precipitate was recovered by filtration and washed with methanol to obtain 32 g of the desired product. The melting point thereof was 92 to 93.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04133686 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-3b840c488f5449359c83fb68d3ee5019 |
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| Source note | uspto-grants-1979_01 |
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