HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413966Generated: November 4, 2026
Triethylamine → L-Valine, N-[2-chloro-4-(trifluoromethyl)phenyl]-
https://huagongshe.com/reaction/1413966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-Valine, N-[2-chloro-4-(trifluoromethyl)phenyl]- | HCID 156536 | — |
| Reactant | 3-Benzyl-1-pyrrolylmethanol | HCID 54343081 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | L-Valine, N-[2-chloro-4-(trifluoromethyl)phenyl]- | HCID 156536 | — |
| Product | 3-Benzylpyrrolylmethyl 2-(2-chloro-4-trifluoromethylphenylamino)-3-methylbutanoate | HCID 20289286 | — |
Reaction Steps
To a stirred solution of 3-benzylpyrrolylmethyl alcohol (0.99 mmol) and triethylamine (0.14 g, 1.38 mmol) in ether (about 15 ml), under nitrogen, is added by syringe a solution of the acid chloride of N-(2-chloro-4-trifluoromethylphenyl)valine (1.5 mmol) in ether. The mixture is stirred for 30 minutes and then quenched with saturated aqueous sodium bicarbonate. The ether phase is washed with aqueous sodium bicarbonate, water and brine and filtered through silica. Evaporation of solvent, followed by thin layer chromatography using a circular chromatography, eluting with 20% ether/hexane, gives the 3-benzylpyrrolylmethyl ester of N-(2-chloro-4-trifluoromethylphenyl)valine, [3-benzylpyrrolylmethyl 2-(2-chloro-4-trifluoromethylphenylamino)-3-methylbutanoate].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04252724 |
|---|
| Source dataset | uspto-grants-1981_02 |
|---|
| ORD ID | ord-1155dafd247b4307ba46b67164b40bc9 |
|---|
| Source note | uspto-grants-1981_02 |
|---|