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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425744Generated: October 26, 2026

1,6-Dioxaspiro[2.5]octane → Benzyl({1-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidin-4-yl}methyl)carbamate

https://huagongshe.com/reaction/2425744

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,6-Dioxaspiro[2.5]octaneHCID 160439—
ReactantBenzyl (piperidin-4-ylmethyl)carbamateHCID 14809798—
SolventMethanolHCID 887—
ProductBenzyl({1-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidin-4-yl}methyl)carbamateHCID 5925504849.4%

Reaction Steps

A mixture of benzyl(piperidin-4-ylmethyl)carbamate (7.77 g, 31.3 mmol, Bose, D. Subhas et al., Tetrahedron Lett., 1990, 31, 6903) and 1,6-dioxaspiro[2.5]octane (4.29 g, 37.6 mmol, Satyamurthy, Nagichettiar et al., Phosphorus Sulfur, 1984, 19, 113) in methanol (93 mL) was stirred at room temperature for 20 h. Then the mixture was refluxed for 8 h. After cooling to room temperature, the solvent was removed in vacuo. The residue was chromatographed on a column of silica gel eluting with methanol/dichloromethane (1:20) to give 5.60 g (49%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964727B2
Source datasetuspto-grants-2011_06
ORD IDord-ef1b49d49afc4235abbd70cb4a2982c5
Source noteuspto-grants-2011_06