HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651036Generated: October 31, 2026
Water → 1-phenyl-N-(1,3-thiazol-2-ylmethyl)methanamine
https://huagongshe.com/reaction/651036
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 1,3-Thiazole-2-carbaldehyde | HCID 2734903 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-phenyl-N-(1,3-thiazol-2-ylmethyl)methanamine | HCID 4777619 | 58.9% |
Reaction Steps
A stirred solution of N-benzylamine (0.56 mL, 5.1 mmol) and 2-thiazolecarboxaldehyde (0.55 g, 4.9 mmol) in toluene was heated to reflux for 2 hours with azeotropic removal of water. The solution was cooled to room temperature and concentrated to an oil. This oil was dissolved in 15 mL of ethanol and treated with excess NaBH4 and the mixture stirred overnight. Acetone was added and the mixture stirred 30 minutes and concentrated to a soild mass. This mass was partitioned between 2N aqueous NaOH and 2 portions of ethyl ether. The combined ethereal extracts were washed with water, brine, dried (Na2SO4), filtered, and concentrated. The residue was purified by flash column chromatography on silica gel to provide 0.59 g (57%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06277871B1 |
|---|
| Source dataset | uspto-grants-2001_08 |
|---|
| ORD ID | ord-74db08013dc7466199a32a173adbda77 |
|---|
| Source note | uspto-grants-2001_08 |
|---|