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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901317Generated: October 31, 2026

3,4-dihydro-2H-pyran → Methyl 6-[(2-tetrahydropyranyl)oxymethyl]-5,6,7,8-tetrahydro-2-naphthalenecarboxylate

https://huagongshe.com/reaction/1901317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantMethyl 6-hydroxymethyl-5,6,7,8-tetrahydro-2-naphthalenecarboxylateHCID 13851838—
CatalystSulfuric AcidHCID 1118—
SolventDiethyl EtherHCID 3283—
ProductMethyl 6-[(2-tetrahydropyranyl)oxymethyl]-5,6,7,8-tetrahydro-2-naphthalenecarboxylateHCID 2184432499.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576343
Source datasetuspto-grants-1996_11
ORD IDord-9886009ca187403bb79a0f5ed9b20010
Source noteuspto-grants-1996_11