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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184933Generated: October 31, 2026

Sodium borohydride → HCID 22458855, compound

https://huagongshe.com/reaction/2184933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22458811HCID 22458811—
SolventEthanolHCID 702—
ProductHCID 22458855HCID 2245885566.1%

Reaction Steps

To a solution of N-(9-Ethyl-6-formyl-9H-carbazol-3-yl)-acetamide (50 mg, 0.150 mmol) in EtOH (5 ml) at 0° C. was added NaBH4 (8.5 mg, 0.225 mmol), and after 10 minutes the cooling bath was removed. After 1 hour additional NaBH4 (2 mg) was added, and after stirring 90 minutes water was added, the EtOH removed in vacuo, and the aqueous layer extracted with CH2Cl2. The organic layer was dried (Na2SO4) and concentrated to afford the crude product. Chromatographic purification (silica, 50% EtOAc/Hex) afforded the product as a solid (28 mg, 56% yield). MS m/z @ 337 (m+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399631B1
Source datasetuspto-grants-2002_06
ORD IDord-dbb9095b484f4e7d88e6888690f29c73
Source noteuspto-grants-2002_06