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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191006Generated: November 1, 2026

Acetic Acid → (R)-4-[(1-Methyl-2,2,2-trifluoro-ethylamino)-methyl]-benzonitrile

https://huagongshe.com/reaction/1191006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(2R)-1,1,1-Trifluoropropan-2-amine--hydrogen chloride (1/1)HCID 44593757—
SolventMethanolHCID 887—
Product(R)-4-[(1-Methyl-2,2,2-trifluoro-ethylamino)-methyl]-benzonitrileHCID 5982882327.2%

Reaction Steps

Add sodium cyanoborohydride (3.36 g, 53.5 mmol) to a solution of 4-cyanobenzaldehyde (1.75 g, 13.35 mmol) and (R)-1-methyl-2,2,2-trifluoro-ethylamine hydrochloride (2 g, 13.37 mmol) in methanol (17 mL) containing acetic acid (1.53 mL, 26.75 mmol). Stir the mixture at room temperature overnight. Partition the mixture between 1N aqueous NaOH/DCM (1:1, 500 mL) and extract the aqueous layer twice with DCM. Dry the combined organic extracts over MgSO4, concentrate in vacuo and purify by chromatography on silica gel (120 g) eluting with hexane/EtOAc (19:1, 9:1, 85:15 and 4:1) to obtain the desired intermediate (0.83 g, 27%). MS (ES+) m/z: 229 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680091B2
Source datasetuspto-grants-2014_03
ORD IDord-e6d71cbd1e324fadb2d0c77c10a71133
Source noteuspto-grants-2014_03