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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193622Generated: November 1, 2026

Ethyl Acetate → HCID 54263880, compound

https://huagongshe.com/reaction/1193622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantHydrideHCID 166653—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 86742790HCID 86742790—
SolventDiethyl EtherHCID 3283—
ProductHCID 54263880HCID 54263880—

Reaction Conditions

Temperature-65 °C

Reaction Steps

A 250 ml 3-necked flask is fitted with a stirrer, a dripping funnel, a nitrogen inlet and a thermometer. In the flask is placed a solution of 379.5 mg (10 mmol) of lithium aluminum hydride in 30 ml of dry diethyl ether. The solution is cooled to -65° C. under nitrogen and a solution of 3.3441 g (10 mmol) of ethyl-4-((4,4-dimethylchroman-6-ylethynyl)benzoate in 15 ml of dry ether is added dropwise at a rate such that the temperature does not exceed -60° C. The mixture is stirred at -30° C. for 1 hour and the excess hydride is then destroyed by the addition of 300 mg (3.4 mmol) of ethyl acetate. The reaction mixture is then hydrolyzed by adding 3 ml of saturated ammonium chloride solution and allowing the temperature to rise to room temperature. The mixture is then filtered and the residue washed with ether. The ether layer is then washed with saturated sodium chloride solution, dried (MgSO4) and then concentrated in vacuo. The residue is purified by chromatography followed by recrystallization to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810804
Source datasetuspto-grants-1989_03
ORD IDord-ca5f2f59863242819afd0d2a4acada23
Source noteuspto-grants-1989_03