HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633955Generated: October 31, 2026
Sodium Chloride → 3-{4-[(4-Tert-butylphenylamino)methyl]benzoylamino}propionic acid methyl ester
https://huagongshe.com/reaction/1633955
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 4-Tert-Butylaniline | HCID 69861 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-(4-Formylbenzoylamino)propionic acid methyl ester | HCID 16100325 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-{4-[(4-Tert-butylphenylamino)methyl]benzoylamino}propionic acid methyl ester | HCID 16100341 | 30% |
Reaction Steps
The above 3-(4-formylbenzoylamino)propionic acid methyl ester (2.0 g, 8.5 mmol) was dissolved in DMF (20 mL). Triethyl orthoformate (10 mL), glacial acetic acid (1 mL), sodium cyanoborohydride (0.81 g, 12.8 mmol) and 4-tert-butylaniline 1.27 g, 8.5 mmol) were added and the resulting mixture was stirred at room temperature for 16 hours. The mixture was added saturated aqueous sodium chloride (100 mL) and the mixture was extracted with ethyl acetate (3×100 mL). The combined organic extracts were washed with saturated aqueous sodium chloride (3×100 mL). The organic phase was dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with a mixture of ethyl acetate and heptane (1:1) to afford 0.87 g (30%) of 3-{4-[(4-tert-butylphenylamino)methyl]benzoylamino}propionic acid methyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06503949B1 |
|---|
| Source dataset | uspto-grants-2003_01 |
|---|
| ORD ID | ord-476916ddc9e54c038baab9b6c2ce9b1a |
|---|
| Source note | uspto-grants-2003_01 |
|---|