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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973968Generated: October 29, 2026

Tetrahydrofuran → HCID 14054080, compound

https://huagongshe.com/reaction/973968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Butyn-1-olHCID 12991—
ReactantHCID 86745224HCID 86745224—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 14054080HCID 14054080—

Reaction Steps

To a solution of 2.43 ml 0.0325 mol) but-2-yn-1-ol and 3.97 g (0.0325 mol of 4-dimethylaminopyridine in 35 ml tetrahydrofuran is added dropwise, at 0°-5° C., a solution of 7.95 g 0.0325 mol 2-(4-chlorophenyl-3,3-dimethylbutyryl chloride in 25 ml tetrahydrofuran. The reaction mixture was allowed to warm to room temperature and after one and a half hours worked up as follows: after removal of the tetrahydrofuran in vacuo, it was treated with water and stirred with ether, the ether phase was dried over magnesium sulphate and concentrated in vacuo. A colourless oil was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066675
Source datasetuspto-grants-1991_11
ORD IDord-055be7d36ea34b998a8f97432033e77c
Source noteuspto-grants-1991_11