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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408590Generated: October 25, 2026

Sulfuric acid magnesium salt (1:1) → 4-[(Benzofuran-6-ylmethyl)-amino]-butyric acid ethyl ester

https://huagongshe.com/reaction/408590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Aminobutyrate ethyl hydrochlorideHCID 12649661—
ReactantBenzofuran-6-carbaldehydeHCID 14354086—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-[(Benzofuran-6-ylmethyl)-amino]-butyric acid ethyl esterHCID 70556474—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 4-amino-butyric acid ethyl ester hydrochloride (1 eq.) in THF was added TEA (2.5 eq.). The mixture was stirred 5 min at 20° C., then benzofuran-6-carbaldehyde (0.95 eq.) and MgSO4 (3 eq.) were added. The reaction was refluxed for 2 h, then cooled to 20° C. and filtered. The filtrate was added to a suspension of NaBH4 (2 to 6 eq.) in MeOH at −15° C. The reaction was stirred for 2 h at −15° C. The reaction was quenched with the addition of aqueous HCl 2N until pH=2. The aqueous layer was washed twice with EtOAc. The organic layers were discarded. Solid KOH was added to the aqueous layer. The crude was extracted three times with EtOAc. The organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure at 20° C. The crude was purified by chromatography on silica gel (elution with DCM/MeOH: 95/5) to afford 4-[(benzofuran-6-ylmethyl)-amino]-butyric acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759334B2
Source datasetuspto-grants-2014_06
ORD IDord-ac60bff47ab3460f836ac051f1ee32e2
Source noteuspto-grants-2014_06