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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602513Generated: October 29, 2026

2-Benzofurancarboxaldehyde → HCID 9927809, compound

https://huagongshe.com/reaction/602513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BenzofurancarboxaldehydeHCID 61341—
ReactantHCID 56953891HCID 56953891—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9927809HCID 992780943%

Reaction Steps

A mixture of 0.1 M solution of (4-amino-2-methylphenyl)-carbamic acid propyl ester (0.35 mL, 0.035 mmol) and 0.1 M solution of benzofuran-2-carbaldehyde (0.35 mL) in tetrahydrofuran (THF) was kept at 55° C. for 60 minutes. Volatiles were removed in vacuo. To the obtained residue 0.2 M sodium cyanoborohydride (NaBH3CN) (0.5 mL) in methanol and acetic acid (0.03 mL) were added. After sonication for 60 minutes the reaction mixture was evaporated in vacuo and the title compound was separated by preparative LC/MS to give 5.1 mg of colorless solid. Yield 43%. LC/MS (m/z) 339.2 ([M+H]+); RT=2.92, (UV, ELSD) 94%, 94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906537B2
Source datasetuspto-grants-2011_03
ORD IDord-ba831cc8c27847a09f75aa65bcf1ffd4
Source noteuspto-grants-2011_03