HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863852Generated: October 30, 2026
Potassium hydride → N-trityl-1-[4-(benzoxazol-2-yl)benzyloxy]-3-(4-phenylbutoxy)-2-propanamine
https://huagongshe.com/reaction/863852
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; 1.1 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 2×. 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 | US05561143 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-76e114dcb8fb40e395173913a5b9f9cf |
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| Source note | uspto-grants-1996_10 |
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