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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111684Generated: October 29, 2026

2-Methyl-2-pentenal → 4-Methylhept-4-en-1-yn-3-ol

https://huagongshe.com/reaction/1111684

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-pentenalHCID 12177—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418486HCID 178418486—
SolventTetrahydrofuranHCID 8028—
Product4-Methylhept-4-en-1-yn-3-olHCID 53730069364.8%

Reaction Steps

To a solution of ethynyl magnesium bromide (prepared from 2.91 g of magnesium) in 100 ml of tetrahydrofuran, was added dropwise 9.8 g of 2-methyl-2-pentenal at a temperature from 0° C to 10° C under cooling with ice-bath. The resulting reaction solution was stirred for 3 hours at room temperature to complete the reaction and then the reaction solution was poured into a saturated ammonium cloride solution with 50 g of ice. After stirring, the solution was extracted twice with 100 ml of ether and the organic layers were combined, and then washed with 50 ml of a saturated sodium chloride solution. After the organic layer had been dried over anhydrous sodium sulfate, the ether was evaporated. The remaining liquid was purified by distillation at reduced pressure to obtain 10.2 g of a colorless oily 1-ethynyl-2-methyl-2-pentenyl alcohol, b.p. 85°-88° C/20 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04118505
Source datasetuspto-grants-1978_10
ORD IDord-c758642d4a244103b3b181cbb7b6cb05
Source noteuspto-grants-1978_10