HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116812Generated: October 25, 2026
Isopropanol → 2-fluoro-4-isopropyl-N-methoxycarbonylaniline
https://huagongshe.com/reaction/2116812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-fluoro-N-methoxycarbonylaniline | HCID 3484174 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 2-fluoro-4-isopropyl-N-methoxycarbonylaniline | HCID 10262568 | 53.3% |
Reaction Steps
2-Fluoro-N-methoxycarbonylaniline (1.00 g, 5.92 mmol) prepared as described in Example 1 was dissolved in 77.6% sulfuric acid (5.00 g) to prepare a solution. Isopropyl alcohol (0.400 g, 6.51 mmol) was added to the solution under a nitrogen atmosphere while stirring and heating the solution at 70° C. The mixture was vigorously stirred for 3 hr. The reaction solution was cooled to room temperature. n-Hexane (10 mL) was then added to the cooled reaction solution to carry out extraction for separation of the mixture into a sulfuric acid layer and an organic layer, and this extraction was carried out once again. The organic layers thus obtained were combined, and the combined organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine in that order. The solvent was then removed from the organic layer by distillation to give 666 mg of 2-fluoro-4-isopropyl-N-methoxycarbonylaniline as an oil. The oil was further subjected to separation and purification by column chromatography on silica gel to give 206 mg of 2-fluoro-4-isopropyl-N-methoxycarbonylaniline (yield 17.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439382B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-aedcec1454ba4c1ea98d44db15d56ad8 |
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| Source note | uspto-grants-2008_10 |
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