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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802070Generated: November 2, 2026

HCID 23600236, compound → HCID 67407596, compound

https://huagongshe.com/reaction/1802070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23600236HCID 23600236—
ReactantHCID 178418373HCID 178418373—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67407596HCID 6740759680%

Reaction Steps

To a solution of 7-(heptyloxy)quinoline-3-carbaldehyde (1.6 g, 5.9 mmol) in THF (30 mL) at 0° C. was added CH3MgI (2 g, 12 mmol, 2 eq.) dropwise over 10 min. The mixture was warmed to it over 8 h. Then, the reaction mixture was quenched (water), extracted (ethyl acetate), washed (brine), dried (Na2SO4), filtered and evaporated to dryness to give the crude product, which was purified by silica gel column chromatography (pet. ether:ethyl acetate, 1:5) to give 1-(7-(heptyloxy)quinolin-3-yl)ethanol as yellow oil (1.35 g, yield 80%). ESI-MS: 288 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349849B2
Source datasetuspto-grants-2013_01
ORD IDord-eb9be36591ce48839d233cefacacceaa
Source noteuspto-grants-2013_01