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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352638Generated: October 25, 2026

Acetyl chloride → 1-(4'-t-Butyldimethylsilyloxy-3'-methoxyphenyl)-1-hexene-3,5-dione

https://huagongshe.com/reaction/2352638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantLithium diisopropylamideHCID 2724682—
ReactantDiethylether hexaneHCID 21584099—
Reactant1-(4'-t-Butyldimethylsilyloxy-3'-methoxyphenyl)-1-butene-3-oneHCID 54529210—
SolventTetrahydrofuranHCID 8028—
Product1-(4'-t-Butyldimethylsilyloxy-3'-methoxyphenyl)-1-hexene-3,5-dioneHCID 5415648334.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1-(4'-t-butyldimethylsilyloxy-3'-methoxyphenyl)-1-butene-3-one (12.8 g, 41.8 mmol) in THF (50 mL) is cooled to -78° C. under an argon atmosphere. Lithium di-isopropyl amide (83.5 mmol, in 50 mL THF) is slowly added to the reaction mixture. The reaction is stirred at -78° C. for 30 minutes. Acetyl chloride (16.4 g, 209 mmol) dissolved in THF (20 mL) is then added to the reaction over a 30 minute period. The reaction is quenched with aqueous HCl. The layers are separated, and the aqueous layer is washed with ethyl acetate. The combined organic layers are washed with saturated aqueous sodium bicarbonate, dried over MgSO4, and evaporated to give a red oil. Flash chromatography (ethyl ether/hexane 2:8) afford 5.0 g (34%) of 1-(4'-t-butyldimethylsilyloxy-3'-methoxyphenyl)-1-hexene-3,5-dione, mp=81°-85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877881
Source datasetuspto-grants-1989_10
ORD IDord-78cb869710eb4e98b9f0a12df0cbeb34
Source noteuspto-grants-1989_10