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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731195Generated: October 26, 2026

1-methyl-1H-imidazole-5-carbaldehyde → (1-Methyl-1H-imidazol-5-yl)(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)methanol

https://huagongshe.com/reaction/731195

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-methyl-1H-imidazole-5-carbaldehydeHCID 573592—
ReactantHCID 178419637HCID 178419637—
SolventTetrahydrofuranHCID 8028—
Product(1-Methyl-1H-imidazol-5-yl)(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)methanolHCID 5783580297.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

4-(2-Tetrahydro-3H-pyranoxy)phenylmagnesium bromide (110 mL, 0.5 M in THF, 55 mmol) was added dropwise to a solution of 1-methyl-1H-imidazole-5-carbaldehyde (4.7 g, 50 mmol) in THF (790 mL) at −78° C. After stirring −78° C. for 2 hours, the reaction was quenched with saturated NH4Cl (aq) and warmed to room temperature. The mixture was extracted with EtOAc (500 mL), and the organic phase was washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give 14 g of the crude product 74.1, which was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582803B2
Source datasetuspto-grants-2009_09
ORD IDord-0726f1e1e6cb44e1aed365d18742bd22
Source noteuspto-grants-2009_09