HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238596Generated: October 28, 2026
Hydrochloric Acid → (4-Benzyloxy-6-fluoro-naphthalen-2-yl)-methanol
https://huagongshe.com/reaction/238596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 4-Benzyloxy-6-fluoro-naphthalene-2-carboxylic acid methyl ester | HCID 59326585 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Benzyloxy-6-fluoro-naphthalen-2-yl)-methanol | HCID 59326474 | 93% |
Reaction Steps
To the slurry of lithium aluminum hydride (1.4 g, 36.9 mmol) in tetrahydrofuran (30 mL) was added a solution of 4-benzyloxy-6-fluoro-naphthalene-2-carboxylic acid methyl ester (5.8 g, 18.7 mmol) in tetrahydrofuran (30 mL) at 0° C. under a nitrogen atmosphere. After being heated at 60° C. for 1 hour under a nitrogen atmosphere, the resulting mixture was cooled to 0° C. and 1 N hydrochloric acid was added to quench the reaction. The aqueous layer was extracted with diethyl ether (50 mL×4). The combined organic layers were dried over sodium sulfate and concentrated in vacuo to give (4-benzyloxy-6-fluoro-naphthalen-2-yl)-methanol (4.9 g, 93%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642629B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-8167e80975974b1295aa0707c9c5ba89 |
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| Source note | uspto-grants-2014_02 |
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