HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61517Generated: October 25, 2026
p-Toluenesulfonic acid → 5-Chlorobenzoxazole
https://huagongshe.com/reaction/61517
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | 2-Amino-4-chlorophenol | HCID 7265 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chlorobenzoxazole | HCID 28398 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09441254B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-3db72312b4db4d1b8a889bf79aad3f34 |
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| Source note | uspto-grants-2016_09 |
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