HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445875Generated: October 30, 2026
Ethyl 2-methylbenzo[d]oxazole-7-carboxylate → (2-Methyl-1,3-benzoxazol-7-yl)methanol
https://huagongshe.com/reaction/445875
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-methylbenzo[d]oxazole-7-carboxylate | HCID 12157468 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Methyl-1,3-benzoxazol-7-yl)methanol | HCID 58566559 | 68% |
Reaction Steps
To a solution of ethyl 2-methylbenzo[d]oxazole-7-carboxylate (743) (1.27 g, 6.19 mmol) in tetrahydrofuran (61 mL) at 0° C. was added lithium aluminum hydride (7.43 mL, 7.43 mmol, 1M in tetrahydrofuran). The reaction was stirred at 0° C. for 1 hour and quenched with 0.6 mL of water, 0.6 mL of 15% NaOH and 1.8 mL of water. The reaction was warmed to room temperature and diluted with diethyl ether. Magnesium sulfate was added and the solution was filtered, washed with diethyl ether, and the solvent was removed in vacuo to provide (2-methylbenzo[d]oxazol-7-yl)methanol (744) (0.687 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476308B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-b3fa9ea86a184523bdfe5ccbc685e6fe |
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| Source note | uspto-grants-2013_07 |
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