HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732191Generated: October 30, 2026
Propanal → Methyl 3-[4-({3-[[(4-phenyl-1,3-thiazol-2-yl)methyl](propyl)amino]benzyl}oxy)phenyl]propanoate
https://huagongshe.com/reaction/732191
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propanal | HCID 527 | — |
| Reactant | 4-Phenyl-1,3-thiazole-2-carbaldehyde | HCID 3538814 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methyl 3-{4-[(3-aminobenzyl)oxy]phenyl}-propanoate | HCID 23143302 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-[4-({3-[[(4-phenyl-1,3-thiazol-2-yl)methyl](propyl)amino]benzyl}oxy)phenyl]propanoate | HCID 23143254 | 78.5% |
Reaction Steps
To a mixture of 4-phenyl-1,3-thiazole-2-carbaldehyde (210 mg, 1.1 mmol), methyl 3-{4-[(3-aminobenzyl)oxy]phenyl}-propanoate (285 mg, 1.0 mmol), acetic acid (0.2 mL) and 1,2-dichloroethane (5 mL) was added sodium triacetoxyborohydride (0.6 g, 2.8 mmol) under ice-cooling, and the mixture was warmed to room temperature and stirred for 1 hr. Propanal (200 mg, 3.4 mmol) was added to the reaction mixture, and the mixture was further stirred at room temperature for 1 hr. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:19-1:2 in volume ratio) to give the title compound (393 mg, yield 78%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585880B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-fcf9313ff1bb41baac2c41f165c80b30 |
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| Source note | uspto-grants-2009_09 |
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