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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265280Generated: October 31, 2026

Water → 2-Naphthalen-1-yl-5-phenyl-1-(2-trimethylsilanyl-ethoxycarbonylamino)-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1265280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazinecarboxylic acid 2-trimethylsilanyl-ethyl esterHCID 10241327—
Reactant2-(Naphthalene-1-carbonyl)4-oxo-4-phenyl-butyric acid ethyl esterHCID 20582751—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product2-Naphthalen-1-yl-5-phenyl-1-(2-trimethylsilanyl-ethoxycarbonylamino)-1H-pyrrole-3-carboxylic acid ethyl esterHCID 2058274995.9%

Reaction Steps

A solution of 2-(Naphthalene-1-carbonyl)-4-oxo-4-phenyl-butyric acid ethyl ester (1 g, 2.77 mmol) in toluene (6.5 mL) was treated with Hydrazinecarboxylic acid 2-trimethylsilanyl-ethyl ester (599 mg, 3.34 mmol) and p-toluene sulfonic acid (33 mg). The resulting solution was heated to reflux, with the azeotropic removal of water (Dean Stark trap), under Ar for 6 h, cooled to rt and concentrated in vacuo to afford 2-Naphthalen-1-yl-5-phenyl-1-(2-trimethylsilanyl-ethoxycarbonylamino)-1H-pyrrole-3-carboxylic acid ethyl ester (1.33 g), which was not purified, but used immediately in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545108B1
Source datasetuspto-grants-2003_04
ORD IDord-440a9d322b4a4962a2a9f15e7e05f866
Source noteuspto-grants-2003_04