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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantHexaneHCID 8058—
Reactant2-fluoro-N-methoxycarbonylanilineHCID 3484174—
SolventSulfuric AcidHCID 1118—
Product2-fluoro-4-isopropyl-N-methoxycarbonylanilineHCID 1026256853.3%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439382B2
Source datasetuspto-grants-2008_10
ORD IDord-aedcec1454ba4c1ea98d44db15d56ad8
Source noteuspto-grants-2008_10