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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429011Generated: November 3, 2026

Acetic Acid → cis-(2-Benzhydryl-tetrahydropyran-4-yl)-(4-fluorobenzyl)-amine

https://huagongshe.com/reaction/1429011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactantcis-(2-Benzhydryl-tetrahydropyran-4-yl)-amineHCID 68717496—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Productcis-(2-Benzhydryl-tetrahydropyran-4-yl)-(4-fluorobenzyl)-amineHCID 6663163479.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of cis-4-amino-2-diphenylmethylpyran 6a (0.2 g, 0.75 mmol), 4-fluorobenzaldehyde (0.83 g, 0.67 mmol) and glacial acetic acid (0.45 g, 0.75 mmol) in 1,2-dichloroethane (20 ml), was added portion wise NaCNBH3 (0.57 g, 0.9 mmol) dissolved in methanol (5 ml). After 4 hr, water was added to quench the reaction and the mixture was stirred for 30 minutes at 0° C. Then the mixture was made basic with saturated aqueous NaHCO3 and extracted thrice with methylene chloride (3×30 ml). The combined organic phases were washed with brine, water and dried over anhydrous Na2SO4. Solvent was removed in vacuo to collect the crude residue, which was purified by flash chromatography (Hexane/Ethyl Acetate/Triethylamine 3:2:0.2) to give cis-2-diphenylmethyl-4-(4-fluorobenzylamino)-tetrahydropyran 7a (0.20 g, 72.6%) as a liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937189B2
Source datasetuspto-grants-2015_01
ORD IDord-68b746a852b142f38aeda9623d44ff47
Source noteuspto-grants-2015_01