HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886933Generated: October 31, 2026
Ethyl Acetate → 2-(4-Chlorobenzylthio)benzo[d]oxazol-5-amine
https://huagongshe.com/reaction/1886933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(4-Chlorobenzylthio)-5-nitrobenzo[d]oxazole | HCID 67332584 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 2-(4-Chlorobenzylthio)benzo[d]oxazol-5-amine | HCID 61359274 | 94% |
Reaction Steps
To a suspension of 2-(4-chlorobenzylthio)-5-nitrobenzo[d]oxazole (220 mg, 0.70 mmol) in ethanol/water (5 mL/5 mL) at 90° C. was added ammonium chloride (75 mg, 1.4 mmol), followed by iron powder (192 mg, 3.44 mmol). The resulting mixture was stirred for 4 h at 90° C. After cooling, ethyl acetate was added and the solution was passed through a pad of Celite®. The organic layer was then washed with brine, dried over anhydrous MgSO4 and evaporated to afford 190 mg (94%) of the title compound (LCMS RT=6.54 min, MH+ 290.9)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501713B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-1059e2e45f614288a76a56b4e2d4dbe5 |
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| Source note | uspto-grants-2013_08 |
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