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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | (4-Iodobutyl)benzene | HCID 12709818 | — |
| Reactant | N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-hydroxy-2-propanamine | HCID 19420787 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-(4-phenylbutoxy)-2-propanamine | HCID 19420792 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05534532 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-3800d536b0764b818291d1eb14bacd76 |
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| Source note | uspto-grants-1996_07 |
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