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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734688Generated: November 1, 2026

Potassium hydride → N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-(4-phenylbutoxy)-2-propanamine

https://huagongshe.com/reaction/1734688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium hydrideHCID 82127—
Reactant(4-Iodobutyl)benzeneHCID 12709818—
ReactantN-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-hydroxy-2-propanamineHCID 19420787—
SolventTetrahydrofuranHCID 8028—
ProductN-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-(4-phenylbutoxy)-2-propanamineHCID 19420792—

Reaction Conditions

Temperature20 °C

Reaction Steps

N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-hydroxy-2-propanamine (0.4 g; 0.74 mmol) is added to a suspension of potassium hydride (0.12 g; 1. mmol; 35% suspension in oil) in dry THF (4 ml) at 0° C. The reaction is stirred for 15 minutes at 20° C. 4-Phenyl-1-butyl iodide (0.21 g; 0.81 mmol) is added and the reaction mixture stirred for 15 hours. The reaction is quenched with MeOH, diluted with CH2Cl2 and washed with water 2x. The organic phase is dried (Na2SO4), concentrated and purified by column chromatography with 80% CH2Cl2 /20% petroleum ether to yield N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-(4-phenylbutoxy)-2-propanamine as an oil which is used directly in Step F.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534532
Source datasetuspto-grants-1996_07
ORD IDord-3800d536b0764b818291d1eb14bacd76
Source noteuspto-grants-1996_07