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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006753Generated: November 1, 2026

Propargyl alcohol → HCID 22672768, compound

https://huagongshe.com/reaction/1006753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantAmmonium ChlorideHCID 25517—
Reactant6-Bromo-N-butyl-N-methylhexanamideHCID 22672753—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 22672768HCID 22672768—

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of 1.77 ml of propargyl alcohol, 30 ml of tetrahydrofuran and 7.5 ml of hexamethyl phosphotriamide cooled to −60° C. was admixed with 37.5 ml of a 1.6M solution of butyl-lithium in hexane and after stirring for 45 minutes at −30° C., 7 g of the product of Step A in solution in 7 ml of tetrahydrofuran were added. The mixture was stirred for 16 hours at ambient temperature and then poured into a saturated solution of ammonium chloride and extracted with ethyl acetate. The organic phase was washed with 2N hydrochloric acid and with a saturated solution of sodium bicarbonate, dried and evaporated to dryness. The 5.78 g of residue were chromatographed on silica (eluant: methylene chloride—ethyl acetate 70-30, then methylene chloride—isopropanol 95-5) to obtain 1.65 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790971B1
Source datasetuspto-grants-2004_09
ORD IDord-6ec83bbc97554cc9a94de5176dc76ba8
Source noteuspto-grants-2004_09