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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76217Generated: October 29, 2026

Benzaldehyde → Benzyl({2-[4-(4-fluorophenyl)oxan-4-yl]ethyl})amine

https://huagongshe.com/reaction/76217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHCID 68314438HCID 68314438—
SolventDichloromethaneHCID 6344—
ProductBenzyl({2-[4-(4-fluorophenyl)oxan-4-yl]ethyl})amineHCID 68314456—

Reaction Steps

To a solution of 2-[4-(4-fluorophenyl)oxan-4-yl]ethan-1-amine (250 mg, 1.12 mmol) in anhydrous CH2Cl2 (5 ml) and NA2SO4 (159 mg, 1.12 mmol) at rt was added benzaldehyde (0.17 ml, 1.68 mmol). The reaction was stirred overnight. The reaction mixture was filtered and concentrated. The residue was dissolved in 5 ml MeOH at 0° C. and NaBH4 added in one portion (51 mg, 1.34 mmol). The reaction was stirred at 0° C. for 1 h. The solution was then quenched with H2O (10 ml), extracted with CH2Cl2 (3×20 ml), washed with brine (10 ml) and dried over NA2SO4. Purified by normal phase SiO2 chromatography (0 to 10% MeOH/CH2Cl2) to give benzyl({2-[4-(4-fluorophenyl) oxan-4-yl]ethyl})amine as a colorless oil (200 mg, 60%, m/z: 314.2 [M+H]+ observed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835488B2
Source datasetuspto-grants-2014_09
ORD IDord-badf241c33f44666bbd223fe295d6b54
Source noteuspto-grants-2014_09