HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638789Generated: November 4, 2026
Sodium Hydroxide → 3,4-Dihydro-6-(phenylmethoxy)-2-naphthalenecarboxylic acid
https://huagongshe.com/reaction/1638789
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19841196 | HCID 19841196 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3,4-Dihydro-6-(phenylmethoxy)-2-naphthalenecarboxylic acid | HCID 14676197 | 79.8% |
Reaction Steps
Methyl ester of 6-benzyloxy-1-hydroxy-1,2,3,4-tetrahydro-2-naphthoic acid (0.6 g) is dissolved in methanol (50 ml). To the solution is added an aqueous solution (10 ml) of sodium hydroxide (2 g), and the mixture is left standing for 30 minutes at room temperature. The resultant is concentrated under reduced pressure. The concentrate is diluted with water (50 ml). The precipitating crystals are collected by filtration. This product is dissolved in a mixture of dioxane (50 ml) and concentrated hydrochloric acid (2 ml). The mixture is left standing for 5 minutes at 80° C. and then for 30 minutes at room temperature. The resultant is concentrated under reduced pressure. Water (50 ml) is added to the concentrate. The precipitating crystals are collected by filtration to give 7-benzyloxy-1,2-dihydro-3-naphthoic acid (0.45 g) as colorless crystals, followed by recrystallization from a mixture of methanol and acetone to afford colorless needles, m.p. 202°-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04880809 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-c2d425b448184586907ebbbe175e633e |
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| Source note | uspto-grants-1989_11 |
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