HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173299Generated: October 30, 2026
Propylamine → 5-tert-Butyl-2-[(propylamino)methyl]phenol
https://huagongshe.com/reaction/1173299
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-tert-Butyl-2-hydroxybenzaldehyde | HCID 13765272 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-tert-Butyl-2-[(propylamino)methyl]phenol | HCID 10331104 | — |
Reaction Steps
To a mixture of 0.178 g (0.1 mmol) of the product of Step A and 0.206 g (3.5 mmol) of n-propylamine dissolved in 10 mL of CH2Cl2 was added 0.5 g of finely powdered 4 Å molecular sieves. The reaction mixture was stirred under a nitrogen atmosphere at room temperature overnight, then 0.53 g (2.5 mmol) of sodium triacetoxyborohydride was added. The reaction was then stirred an addition 8 h at room temperature, then diluted with CH2Cl2 and MeOH. The mixture was filtered through a pad of Celite filter aid eluted with CH2Cl2, and the filtrate was washed with saturated aqueous NaHCO3. The organic layer was the separated, dried (Na2SO4), filtered and evaporated in vacuo. The residue was purified on a flash chromatography column eluted with CH2Cl2-MeOH—NH4OH (95:4:1) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834062B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-a22a27862ef14d7caa6991d78aa99e75 |
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| Source note | uspto-grants-2010_11 |
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