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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035602Generated: November 4, 2026

Imidazole → 8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehyde

https://huagongshe.com/reaction/2035602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDichloromethaneHCID 6344—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant8-Hydroxy-2-quinolinecarboxaldehydeHCID 599342—
SolventWaterHCID 962—
Product8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehydeHCID 5856708274%

Reaction Steps

A solution of 8-hydroxyquinoline-2-carbaldehyde (10.00 g, 57.75 mmol) and imidazole (8.649 g, 127.0 mmol) in DCM (290 mL, 57.75 mmol) was cooled to 0° C. on an ice bath. TBDMS-Cl (9.574 g, 63.52 mmol) was added and the reaction stirred overnight at ambient temperature. Water was added and the reaction transferred to a separatory funnel. The aqueous phase was extracted 3 times with DCM, the organics combined, followed by washes with water and brine. The combined organic layers were dried over Na2SO4, filtered and concentrated to residue under reduced pressure. The residue was purified by flash column chromatography, eluting with 25% EtOAc/Hexanes to give the product (12.2 g, 74% yield). MS APCI (+) m/z 288.1 (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575145B2
Source datasetuspto-grants-2013_11
ORD IDord-e8aaa53c61a44e2f8f448f2d45c7aa55
Source noteuspto-grants-2013_11