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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514650Generated: November 4, 2026

Sodium borohydride → HCID 66670254, compound

https://huagongshe.com/reaction/1514650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86626939HCID 86626939—
SolventEthanolHCID 702—
ProductHCID 66670254HCID 66670254—

Reaction Steps

A 750 mg portion of ethyl 5-tert-butyl-1-[2-(4-fluorophenyl)ethyl]-4-formyl-2-methyl-1H-pyrrole-3-carboxylate was suspended in 15 ml of ethanol, and 158 mg of sodium borohydride was added at 0° C., followed by stirring at room temperature for 2 hours. The solvent was evaporated under a reduced pressure, chloroform and water were added, and the organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. By evaporating the solvent under a reduced pressure, 754 mg of ethyl 5-tert-butyl-1-[2-(4-fluorophenyl)ethyl]-4-(hydroxymethyl)-2-methyl-1H-pyrrole-3-carboxylate was obtained as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222274B2
Source datasetuspto-grants-2012_07
ORD IDord-0f893527366c4cc5b5a3167ff25c4499
Source noteuspto-grants-2012_07