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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733178Generated: October 26, 2026

Gamma-Butyrolactone → 1,3-Dioxo-6-hydroxy-1(3'-tert-butyl-phenyl)-hexane

https://huagongshe.com/reaction/733178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGamma-ButyrolactoneHCID 7302—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(3-tert-Butylphenyl)ethan-1-oneHCID 13657978—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product1,3-Dioxo-6-hydroxy-1(3'-tert-butyl-phenyl)-hexaneHCID 57839120—

Reaction Steps

To a stirring suspension of NaH (60% in oil, 7.66 g) in ether (480 ml) at 0° C. was added ethanol (479 μL), followed by γ-butyrolactone (6.18 ml). This was followed by dropwise addition of 1-(3-tert-butyl-phenyl)-ethanone (13.5 g) in ether (80 ml). The resulting mixture was allowed to warm to room temperature and stirred for 72 hours. After careful addition of ethanol (10.5 ml), ammonium chloride solution (10 g in 250 ml water) was then added, ether layer was then separated and washed with brine (300 ml), dried over MgSO4 and concentrated in vacuo to give 1,3-dioxo-6-hydroxy-1(3′-tert-butyl-phenyl)-hexane as crude product (18.5 g). This required no purification and was immediately used in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589095B2
Source datasetuspto-grants-2009_09
ORD IDord-44a0741dc5894e7abf0078fe50f4a301
Source noteuspto-grants-2009_09