Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678579Generated: November 2, 2026

Salicylaldehyde → HCID 23136275, compound

https://huagongshe.com/reaction/1678579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantBromocyclopentaneHCID 8728—
ReactantSodium hydrideHCID 24758—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 23136275HCID 2313627525%

Reaction Steps

Salicylaldehyde (1.0 g, 8.2 mmol) was dissolved in DMF (10 mL), cyclopentyl bromide (1.76 mL, 16.4 mmol) and sodium hydride (394 mg, 9.8 mmol) were added thereto, and then the mixture was stirred at room temperature for 2 hours. To the reaction solution was added water, and the reaction mixture was extracted with ethyl acetate. The extract was dried, and then concentrated under reduced pressure. The residue was purified with silica gel column chromatography (hexane/ethyl acetate=100:0 to 90:10) to give an oily matter. The resulting oily matter was dissolved in methanol (10 mL), sodium borohydride (620 mg, 16.4 mmol) was added thereto, and then the mixture was stirred at room temperature for 2 hours. The residue was purified with silica gel column chromatography (hexane/ethyl acetate=100:0 to 70:30) to give the title compound (349 mg, yield 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008525B2
Source datasetuspto-grants-2011_08
ORD IDord-e1c98886a5dd43fcb9d85ee6f6b9c955
Source noteuspto-grants-2011_08