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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859276Generated: October 27, 2026

Acetylene → N-Butyl propiolate

https://huagongshe.com/reaction/1859276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
ReactantPempidineHCID 6603—
ReactantButyl chloroformateHCID 61140—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
ProductN-Butyl propiolateHCID 1136699085%

Reaction Conditions

Temperature40 °C

Reaction Steps

0.42 g (0.36 mmol) of tetrakis(triphenylphosphine)palladium(0), 20 mg (0.16 mmol) of 4-dimethylamino-pyridine and 2.87 g (18.5 mmol) of 1,2,2,6,6-penta-methylpiperidine are introduced into 30 ml of dichloromethane in a 60 ml autoclave under argon. Then 10 bar of acetylene are injected, and the autoclave is heated to 40° C. 5 g (36.6 mmol) of n-butyl chloroformate are pumped in over the course of 10 min, and then acetylene is further injected to 20 bar. The amount of acetylene taken up is replenished hourly over the course of 24 h, and, after cooling, the reaction discharge is flushed with nitrogen and the reaction mixture is distilled. n-Butyl propiolate is isolated in 85% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153786
Source datasetuspto-grants-2000_11
ORD IDord-22efaec56935488392cb6fff9daf2f20
Source noteuspto-grants-2000_11