Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Chloro-3,5-dinitrobenzoic acid | HCID 8377 | — |
| Reactant | 2-Cyclohexylethanol | HCID 20508 | — |
| Reactant | Sulfolane | HCID 31347 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22311653 | HCID 22311653 | — |
Reaction Steps
After charging 50 parts of 4-chloro-3,5-dinitrobenzoic acid, 0.3 part of 98% sulfuric acid, 78 parts of cyclohexaneethanol and 50 parts of sulfolane into a flask, the mixture was heated to 100 to 110° C., and was maintained at the same temperature for 8 to 10 hours. After checking the disapearance of 4-chloro-3,5-dinitrobenzoic acid by HPLC, the reaction mass was cooled to room temperature under atmospheric pressure, and to the mass was 240 parts of methanol, and was stirred for 30 minutes. The resulting mixture was filtrated to obtain crystals, and the crystals were washed with 40 parts of methanol and then dried to obtain 58 parts of 2-cyclohexylethyl 4-chloro-3,5-dinitrobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06951706B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-76d68e3b06264d01ba5acf5412e76e48 |
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| Source note | uspto-grants-2005_10 |
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