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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111969Generated: October 31, 2026

3-Carboxybenzaldehyde → HCID 9980457, compound

https://huagongshe.com/reaction/2111969

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-CarboxybenzaldehydeHCID 12077—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68869657HCID 68869657—
SolventAcetic AcidHCID 176—
ProductHCID 9980457HCID 998045731%

Reaction Steps

N-(3-aminobenzyl)-1,1′-biphenyl-4-carboxamide (20 mg, 0.07 mmol) was dissolved in acetic acid (0.5 ml). 3-Carboxybenzaldehyde (14 mg, 0.09 mmol) was added and then sodium borohydride (11 mg, 0.28 mmol) was added. The mixture was stirred at room temperature for 2 hours and evaporated to dryness. DCM was added into the residue. The mixture was loaded on a column (ISOLUTE® SI, 500 mg/3 ml). It was eluted with DCM, MeOH/DCM (0.5:99.5) and then MeOH/DCM (1:99). The product fractions were combined and the solvent was removed, Re-chromatography of the residue on a column (ISOLUTE® SI, 1 g/6 ml) using DCM, MeOH/DCM (0.5:99.5) and then MeOH/DCM (1:99) as eluant gave 9 mg the desired product, yield 31%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521461B2
Source datasetuspto-grants-2009_04
ORD IDord-6c709838121041e289db0d495d180ef1
Source noteuspto-grants-2009_04