HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729779Generated: October 31, 2026
Hydrochloric Acid → 1,8-Naphthalenedimethanol
https://huagongshe.com/reaction/729779
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Naphthalic anhydride | HCID 6693 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,8-Naphthalenedimethanol | HCID 74846 | — |
Reaction Steps
A 12-L 4-neck flask equipped with a thermocouple, an overhead stirrer, a 2-L addition funnel, and a condenser under N2 was charged with 1,8-naphthalic anhydride (200 g, 1.0 mol) in toluene (2.5 L) at room temperature. The reaction mixture was agitated while adding DIBAL-H (1.5 M in toluene, 2.664 L, 4 mol) via the addition funnel over 1.5 h. The solution was then heated to 95° C. overnight, cooled to 15° C. and then slowly diluted with ethyl acetate (2.2 L) and H2O (2 L) followed by addition of concentrated HCl (320 mL). The resulting suspension was stirred for 30 min at room temperature, filtered, and air dried on the filter for 2 h. The resultant material was in 95% ethanol (1.2 L), stirred at 70° C. for 2 h, and filtered to yield a wet solid which was air dried overnight on the filter and then dried at 70° C. in a vacuum oven to yield (8-hydroxymethyl-naphthalen-1-yl)-methanol as a solid;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582649B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-0209447c49984b3d98376c24500a78c3 |
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| Source note | uspto-grants-2009_09 |
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