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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493369Generated: October 25, 2026

Butyl 3-(p-tert-butylphenoxy)-propionate → 3-p-t-Butyl-phenoxypropanol

https://huagongshe.com/reaction/1493369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl 3-(p-tert-butylphenoxy)-propionateHCID 14423333—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product3-p-t-Butyl-phenoxypropanolHCID 13313735—

Reaction Conditions

Temperature-5 °C

Reaction Steps

This ester 21.0 g was dissolved in 500 ml dry ether and cooled to -5° C. in an ice/acetone bath. To the cold solution was added, cautiously, a slurry of 3.5 g lithium aluminum hydride in 100 ml dry ether. After one hour the excess lithium aluminum hydride was destroyed by the cautious addition of 200 ml ethyl acetate, then 50 ml water. The solution was filtered and the filtrate partitioned between 200 ml ether-200 ml water. The organic layer was removed, dried, and evaporated to a yellow oil which was vacuum distilled (116° C./0.35 mm) over potassium carbonate to a clear colorless oil, 3-p-t-butylphenoxypropanol, 10.1 g (64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021460
Source datasetuspto-grants-1991_06
ORD IDord-886c7ec6d20f4b46b4e5b33dc34860ab
Source noteuspto-grants-1991_06