Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Dodecanol | HCID 8193 | — |
| Reactant | p-Acetoxybenzoyl chloride | HCID 2756254 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 19824476 | HCID 19824476 | 68.4% |
Reaction Steps
In 10 ml of pyridine was dissolved 2.0 g of 4-acetoxybenzoic acid chloride, and 2.4 g of dodecyl alcohol was added to the solution. Reaction was carried out at room temperature with stirring. The reaction mixture was treated by customary procedures to obtain 2.4 g of dodecyl 4-acetoxybenzoate. In the same manner as described in Referential Example 13, the acetoxy group was selectively isolated to quantitatively obtain dodecyl 4-hydroxybenzoate. This ester was dissolved in 20 ml of pyridine and a solution of 2.2 g of 3-chloro-4-benzyloxybenzoic acid chloride in 20 ml of pyridine was added to the above solution. The mixture was reacted at room temperature with stirring overnight and the reaction mixture was treated by customary procedures to obtain 3.3 g of 4'-dodecyloxycarbonylphenyl 3-chloro-4-benzyloxybenzoate. In the same manner as described in Referential Example 10, this ester was catalytically reduced to obtain 2.7 g of 4'-dodecyloxycarbonylphenyl 3-chloro-4-hydroxybenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05045228 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-364bc63f61914de69f5c249dbd301dcc |
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| Source note | uspto-grants-1991_09 |
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