HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611931Generated: November 2, 2026
Methyl iodide → 4-Methoxybenzo[d]oxazol-2-amine
https://huagongshe.com/reaction/1611931
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Hydroxy-2-aminobenzoxazol | HCID 21865052 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methoxybenzo[d]oxazol-2-amine | HCID 22252244 | 69.2% |
Reaction Steps
To a stirred solution of 10 g (66 mmol) 2-amino-benzooxazol-4-ol in 100 ml tetrahydrofuran at room temperature was added portionwise 3.49 g (79.9 mmol) sodium hydride (55% dispersion in oil), and the mixture was then stirred for 1 h at 50° C. A solution of 14.5 ml (233 mmol) iodomethane in 500 ml tetrahydrofuran was then added dropwise over 3 h, while the reaction mixture was maintained at 50° C. The mixture was then poured onto water and extracted three times with ethyl acetate. The combined organic phases were washed with saturated brine, dried over sodium sulfate, and concentrated in vacuo. Flash chromatography (dichloromethane then 2/98 methanol/dichloromethane) afforded 7.5 g (69%) 4-methoxy-benzooxazol-2-yl-amine as a brown crystalline solid. EI-MS m/e (%): 164 (M+, 100), 149 ([M−CH3]+, 23), 135 (46).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06992083B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-9cc819735c444ffc9635e18473b2f29b |
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| Source note | uspto-grants-2006_01 |
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