Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233661Generated: November 1, 2026

3-Butyn-2-ol → HCID 10421814, compound

https://huagongshe.com/reaction/233661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Butyn-2-olHCID 16239—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 4-oxo-1-piperidinecarboxylateHCID 34767—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 10421814HCID 10421814—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3-butyn-2-ol (42 g, 0.6 mol) in dry THF (800 ml) under nitrogen was cooled with a dry-ice/acetone bath. n-Butyl lithium (390 ml of 2.5M and 230 ml of 1.5M) in hexane was added rapidly, dropwise. The suspension became gelatinous and another 800 mls of dry THF was added. The reaction was stirred at approximately -78° C. for 1 hour and then at 0° C. for 20 minutes. The reaction was cooled to -78° C. and 1-ethoxycarbonyl-4-piperidinone (104 g, 0.607 mol) in 300 ml of dry THF was added rapidly dropwise. The reaction mixture was allowed to warm to room temperature and then stirred overnight. The reaction mixture was cooled in an ice-bath, diluted with THF (1.51 ), decomposed with saturated NH4Cl, and the THF layer was washed three times with 200 ml of saturated ammonium chloride. The aqueous layers were back-washed with THF (200 ml×3). The organic layers were combined and dried over MgSO4 and evaporated to give an oil. A one-fifth portion of the oil was purified by flash chromatography on silica gel and elution with 30% ethyl acetate/ether afforded the desired product diol (19.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594000
Source datasetuspto-grants-1997_01
ORD IDord-5f5ed05fec0942f4b4df42ce19e1e4d6
Source noteuspto-grants-1997_01