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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357701Generated: October 29, 2026

tert-Butanol → HCID 18667078, compound

https://huagongshe.com/reaction/357701

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantPropargyl bromideHCID 7842—
ReactantHCID 3089723HCID 3089723—
ReactantPotassium tert-butoxideHCID 23665647—
Catalyst18-Crown-6HCID 28557—
SolventAcetonitrileHCID 6342—
ProductHCID 18667078HCID 18667078—

Reaction Steps

To a solution of N-trifluoroacetyl-N-2-heptylamine(6.33 g, 30 mmol) in CH3CN (75 ml)/t-butanol(0.5 ml) was added 18-crown-6(300 mg) and powdered potassium t-butoxide (3.36 g, 30 mmol). After stirring for 15 min most of the solids had dissolved and propargyl bromide (80% in toluene) (3.5 ml, 31.5 mmol) was then added dropwise. The solution was stirred at 80°-85° C. (oil bath temperature) for 24 h during which time the solution became brown in color and a white solid precipitated. After the reaction mixture had cooled to room temperature, dichloromethane (75 ml) was added and the solids were filtered with suction and washed with dichloromethane. The weight of the solids (KBr) was 3.6 g (theoretical:3.57 g). The combined filtrates were rotary evaporated to give 7.3 g of a dark brown liquid (theoretical yield=7.47 g). The product was not purified but used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840979
Source datasetuspto-grants-1998_11
ORD IDord-140be37318f348fcb9e8137ed7e46615
Source noteuspto-grants-1998_11