Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719663Generated: October 27, 2026

Triethylamine → N-((Methoxycarbonyl)methyl)4-Nitrophenylalanine Methyl Ester

https://huagongshe.com/reaction/719663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl bromoacetateHCID 60984—
ReactantMethyl 4-nitro-L-phenylalaninate hydrochlorideHCID 11715866—
SolventTetrahydrofuranHCID 8028—
ProductN-((Methoxycarbonyl)methyl)4-Nitrophenylalanine Methyl EsterHCID 6857402092%

Reaction Steps

Triethylamine (22 mmol) was added to a suspension of 4-Nitrophenylalanine methyl ester hydrochloride (2) (21 mmol) in THF (50 ml). The mixture was stirred at room temperature for one hour, the triethylamine hydrochloride was filtered off, and the filtrate concentrated to yellow oil. The oil was dissolved in dry THF (50 ml) and to this solution was added triethylamine (60 mmol) and methylbromoacetate (60 mmol), the solution was stirred at room temperature under nitrogen atmosphere for 3 hours, after which the precipitate was filtered off and the filtrate concentrated on vacuum. The residue was dissolved in ethylacetate, washed with H2O, dried (MgSO4) and concentrated on vacuum to give yellow oil. The yield was 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132513B2
Source datasetuspto-grants-2006_11
ORD IDord-1d361a77553743f0b595134964d1542c
Source noteuspto-grants-2006_11