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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395683Generated: October 26, 2026

Diethyl Ether → Ethyl 5-(4-(1-hydroxyethyl)phenyl)-2-benzofurancarboxylate

https://huagongshe.com/reaction/1395683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 5-(4-acetylphenyl)benzofuran-2-carboxylateHCID 20329647—
SolventEthanolHCID 702—
ProductEthyl 5-(4-(1-hydroxyethyl)phenyl)-2-benzofurancarboxylateHCID 20337913—

Reaction Steps

1.2 g of sodium borohydride was added in one portion to a stirred mixture of 15.0 g of 6A, 200 ml of ether and 40 ml of ethanol. The mixture was stirred at room temperature for 2 hours. The solvents were evaporated under reduced pressure. 1.6 liters of water was added to the residue and the mixture was extracted with chloroform. The extract was dried (MgSO4), filtered and the solvent was evaporated under reduced pressure. The residue was dissolved in 150 ml of chloroform. The solution was filtered through charcoal. 400 ml of hexane was added. The solid which formed was collected, recrystallized from a 3/50 v/v mixture of chloroform and hexane and dried in a vacuum oven to give ethyl 5-(4-(1-hydroxyethyl)phenyl)-2-benzofurancarboxylate (6B), mp: 108°-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04205080
Source datasetuspto-grants-1980_05
ORD IDord-f2806e7ba71e403b839e4f450a74392b
Source noteuspto-grants-1980_05