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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944877Generated: October 26, 2026

Potassium Hydroxide → 6-(4-Aminophenyl)hex-5-yn-1-ol

https://huagongshe.com/reaction/1944877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2,2,2-trifluoro-N-(4-(6-hydroxyhex-1-yn-1-yl)phenyl)acetamideHCID 57516938—
SolventIsopropanolHCID 3776—
Product6-(4-Aminophenyl)hex-5-yn-1-olHCID 11229247—

Reaction Steps

A solution of Intermediate 39 (8.5 mmol) in IPA (20 mL) was added to a 100° C. solution of potassium hydroxide (1.4 g, 26 mmol) in IPA (150 mL). The mixture was henceforth heated to reflux for 3.5 hours before being concentrated to drying under reduced pressure. The residue was partitioned between water and dichloromethane. The aqueous phase was extracted three times with dichloromethane. The combined extracts were concentrated to dryness under reduced pressure, and the resulting residue was purified via automated flash silica gel chromatography, using a 25 g Silicycle SiliSep flash column (hexanes/ethyl acetate). Concentration of the desired fractions under reduced pressure provided the title compound as a pale blond oil. ES/MS calcd. for C12H16NO+: 190.1. Found m/z=190.2 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394829B2
Source datasetuspto-grants-2013_03
ORD IDord-88bea529e1da43ad9940a5f38adef675
Source noteuspto-grants-2013_03