Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065143Generated: October 31, 2026

Hydrochloric Acid → HCID 4651150, compound

https://huagongshe.com/reaction/1065143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl acetoneHCID 17355—
Reactant(Triethylsilyl)acetyleneHCID 637947—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 4651150HCID 4651150—

Reaction Steps

8 Parts by volume of 2.5 molar n-butyl lithium is added to a solution of 3.1 parts of triethylsilyl acetylene in 20 parts by volume of ethyl ether at -30° C. The resulting solution is allowed to warm to room temperature, then it is cooled again to -30° C. and 3 parts of benzyl acetone is added. The reaction mixture is allowed to warm to room temperature and is then stirred for 1 hour. The reaction mixture is poured into ether and dilute hydrochloric acid. The ethereal layer is washed with water and dried over anhydrous sodium sulfate. The ether is removed under reduced pressure and the residual oil is dissolved in 15 parts by volume of dimethylformamide containing 2 parts of powdered potassium fluoride. This reaction mixture is stirred and heated at 70°-80° C. for 1 hour, after which time it is diluted with water and extracted with ether. The ether layer is separated and washed with water and dried over anhydrous sodium sulfate. The ether is removed under reduced pressure and the residue is chromatographed on silica gel using 30% ethyl acetate/hexane as eluent to provide 3-methyl-3-hydroxy-5-phenyl-1-pentyne.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04328355
Source datasetuspto-grants-1982_05
ORD IDord-3eb3aea2c7ea4cc790b0593aaa222ffa
Source noteuspto-grants-1982_05