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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477619Generated: November 2, 2026

Ethanol → HCID 84681537, compound

https://huagongshe.com/reaction/1477619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 84015811HCID 84015811—
SolventAcetic AcidHCID 176—
ProductHCID 84681537HCID 8468153799%

Reaction Steps

To an ethanol solution (2.0 mL) of 2-(trifluoromethyl)benzofuran-5-carbaldehyde (220 mg, 1.03 mmol) synthesized in Reference Synthesis Example 95, sodium borohydride (115 mg, 3.05 mmol) was added and the resultant solution was stirred at 70° C. for 1 hour and 30 minutes. After completion of the reaction, the reaction solution was cooled to room temperature and acetic acid was added to the cooled solution, followed by concentrating the resultant mixture under reduced pressure. To the obtained residue, water was added and extraction with dichloromethane from the resultant mixture was performed. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain the title compound (219 mg, yield 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-08bc947a43ca404d8db44e14264a67dc
Source noteuspto-grants-2016_08