HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235529Generated: October 30, 2026
Propanal → N2-Mesityl-N7,N7-dipropyl-1,3-benzoxazole-2,7-diamine
https://huagongshe.com/reaction/2235529
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propanal | HCID 527 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | N-Mesityl-7-nitro-1,3-benzoxazol-2-amine | HCID 68581419 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N2-Mesityl-N7,N7-dipropyl-1,3-benzoxazole-2,7-diamine | HCID 58896475 | — |
Reaction Steps
To a flask was added 0.10 g (0.34 mmol) of N-mesityl-7-nitro-1,3-benzoxazol-2-amine and 40 ml of methanol. The flask was purged with nitrogen followed by the addition of 0.01 g of 10% palladium on carbon. The flask was evacuated and pressurized to 2-3 psig hydrogen and stirred for 1 h. After completion as determined by HPLC, the reaction was filtered through GF/F filter paper. The filtrate was transferred to round bottom flask and 0.1 ml (1.7 mmol) of propionaldehyde, 0.1 g (1.7 mmol) of NaBH3CN and 1 ml of acetic acid were added. The mixture was stirred overnight, then diluted with ethyl acetate and washed with water. The organic phase was dried over magnesium sulfate. Filtration, removal of solvent and purification of the residue via Biotage chromatography eluting with 5% methanol/dichloromethane gave 0.11 g (90% for 2 steps) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714009B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-3c1f45537b2f4cacad0bf73b85e3ecf9 |
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| Source note | uspto-grants-2010_05 |
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