HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53955Generated: October 30, 2026
3,4-dihydro-2H-pyran → Methyl 6-[(2-tetrahydropyranyl)oxymethyl]-5,6,7,8-tetrahydro-2-naphthalenecarboxylate
https://huagongshe.com/reaction/53955
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Methyl 6-hydroxymethyl-5,6,7,8-tetrahydro-2-naphthalenecarboxylate | HCID 13851838 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 6-[(2-tetrahydropyranyl)oxymethyl]-5,6,7,8-tetrahydro-2-naphthalenecarboxylate | HCID 21844324 | 99.3% |
Reaction Steps
10.0 g of methyl 6-hydroxymethyl-5,6,7,8-tetrahydro-2-naphthalenecarboxylate was added to 3.82 g of 2,3-dihydropyrane. After further adding 5 drops of concentrated sulfuric acid, the resulting mixture was stirred for 1 hour. To this were further added 1.00 g of 2,3-dihydropyrane and 3 drops of concentrated sulfuric acid, followed by stirring for 5 hours. The resulting reaction mixture was mixed with 100 ml of diethyl ether, and the mixture was washed with saturated sodium bicarbonate aqueous solution, water and saturated sodium chloride aqueous solution in that order, followed by drying. By distilling off the solvent, 13.72 g of methyl 6-[(2-tetrahydropyranyl)oxymethyl]-5,6,7,8-tetrahydro-2-naphthalenecarboxylate was obtained in the form of yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05620991 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-b72212d7812a47658335f243240b1f4b |
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| Source note | uspto-grants-1997_04 |
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