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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488945Generated: October 29, 2026

Acetaldehyde → HCID 22268711, compound

https://huagongshe.com/reaction/488945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22268778HCID 22268778—
SolventMethanolHCID 887—
ProductHCID 22268711HCID 22268711—

Reaction Steps

Methyl 3-amino-5-(trifluoromethyl)benzoate (cf. procedures (116a) and (80a); 177 mg, 0.81 mmol) was dissolved in MeOH (12 mL) and the resulting solution was charged successively with acetaldehyde (0.045 mL, 0.81 mmol) and sodium cyanoborohydride (64 mg, 1.01 mmol). The reaction was stirred at RT for 12 h, concentrated in vacuo, and diluted with EtOAc. The organic phase was washed with sat. NaHCO3, water (2×), and brine before being dried (Na2SO4), filtered, and concentrated in vacuo. This product was dissolved in 3:1 THF/MeOH (12 mL) and the resultant solution was charged with lithium hydroxide (3 mL of a 1N solution). The reaction was stirred for 14 h, acidified with 1N, and extracted with EtOAc (2×). The organic extracts were combined, washed with water, washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide 3-ethylamino-5-(trifluoromethyl)benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974836B2
Source datasetuspto-grants-2005_12
ORD IDord-6457e830b1ec492ca16c195a550dd471
Source noteuspto-grants-2005_12