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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515505Generated: October 26, 2026

p-Toluenesulfonic acid → 5-Chlorobenzoxazole

https://huagongshe.com/reaction/515505

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantPeracetic AcidHCID 6585—
Reactant2-Amino-4-chlorophenolHCID 7265—
SolventTetrahydrofuranHCID 8028—
Product5-ChlorobenzoxazoleHCID 28398—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a 250 mL 3-neck round bottom flask equipped with a distillation head, glass stopper, septum, thermocouple and magnetic stir bar was charged 2-amino-4-chlorophenol (20.00 g, 0.139 mol). The solid was dissolved in THF (60 mL) and p-TsOH (0.265 g, 1.39 mmol) was added. The brown solution was warmed to 60° C. over 10 min and aged for 90 min. HPLC assay of the reaction mixture showed 1 LCAP unreacted starting material. The temperature was increased from 60° C. to 74° C., and at 63° C. solvent distillation began. A total of 58 mL was collected during the first distillation. The mixture was diluted with THF (60 mL) and a total of 67 mL of solvent was removed between 71 and 84° C. The mixture was again diluted with THF (60 mL) and 61 mL of solvent was removed between 74 and 114° C. The dark brown solution was cooled to room temperature. The final mass of the solution was 27.96 g. Analysis of the crude stream by 1H NMR showed 0.1 wt % MeOH present in the sample. 1H NMR (500 MHz, CDCl3): δ=8.10 (s, 1H), 7.76 (d, J=1.5 Hz, 1H), 7.50 (d, J=8.7 Hz, 1H), 7.36 ppm (dd, J=8.7, 1.7 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108959B2
Source datasetuspto-grants-2015_08
ORD IDord-63f3f55979bd463e8e9171e0bb73c655
Source noteuspto-grants-2015_08