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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171632Generated: October 31, 2026

Tetrahydrofuran → HCID 68308536, compound

https://huagongshe.com/reaction/2171632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 86686209HCID 86686209—
SolventEthyl AcetateHCID 8857—
ProductHCID 68308536HCID 6830853671.1%

Reaction Steps

Ethyl 3-(2-ethoxy-2-oxoethyl)benzoate (1.41 g) was mixed with THF (20 ml), and lithium borohydride (260 mg) was added thereto at 0° C., followed by stirring at room temperature overnight. A saturated ammonium chloride solution and EtOAc were added to the reaction mixture at 0° C. The organic layer was washed with water and saturated brine, dried over Na2SO4, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (EtOAc/hexane) to obtain ethyl 3-(2-hydroxyethyl)benzoate (824 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051283B2
Source datasetuspto-grants-2015_06
ORD IDord-beb09baeb6534ea2a00b74af1393802e
Source noteuspto-grants-2015_06