HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372258Generated: October 31, 2026
Dicyclohexylcarbodiimide → 3-Fluoro-4-(2-methyloctanoyl) phenyl-3-fluoro-4-heptyloxy benzoic acid
https://huagongshe.com/reaction/2372258
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | (+)-3-Fluoro 4-(2-methyloctanoyl) phenol | HCID 15027241 | — |
| Reactant | 3-Fluoro-4-heptyloxy benzoic acid | HCID 15027242 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Fluoro-4-(2-methyloctanoyl) phenyl-3-fluoro-4-heptyloxy benzoic acid | HCID 67852796 | 56.5% |
Reaction Steps
Into a flask were charged 1.2 g (4.76 mmol) of (+)-3-fluoro 4-(2-methyloctanoyl) phenol, 1.51 g (5.94 mmol) of 3-fluoro-4-heptyloxy benzoic acid, 76.7 mg (0.63 mmol) of N,N-dimethylamino pyridine and 30 ml of dried methylene chloride, which were slightly heated with stirring to form a homogeneous solution. Then, the solution was added with 1.40 g (6.79 mmol) of dicyclohexyl carbodiimide and stirred over a night. The precipitated white crystal was filtered off, and the resulting filtrate was washed with 2 normal hydrochloric acid, an aqueous solution of 5% sodium hydrogen carbonate and water in this order and dried on magnesium sulfate. After magnesium sulfate was filtered off, the filtrate was concentrated and dried under a reduced pressure to obtain an oil. This oil was purified through a column chromatography and recrystallized with ethanol to obtain 1.02 g (2.69 mmol, yield: 44%) of a white crystal of the objective compound having the aforementioned physical and chemical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05098602 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-df0c5c526fe04e92afc9ffd23c9ed1ec |
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| Source note | uspto-grants-1992_03 |
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