Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325420Generated: October 25, 2026

Diethyl acetonedicarboxylate → Ethyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetate

https://huagongshe.com/reaction/325420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl acetonedicarboxylateHCID 66045—
ReactantSodium AcetateHCID 517045—
ReactantHCID 178451312HCID 178451312—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
ProductEthyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetateHCID 5403425631%

Reaction Steps

Crude t-butyl 5-(m-chlorophenyl)-2-hydroximino-3-oxopentanoate (43 g., 0.15 mol) and diethyl acetonedicarboxylate (28 ml, 30.3 g, 0.15 mol) are placed in a 1 liter round bottom flask and 250 ml of glacial acetic acid added. With stirring, 25 g (0.30 mol) anhydrous sodium acetate is added followed by 26 g Zn dust (94% fine, 0.364 mol) in a portionwise manner so that the exotherm does not bring the reaction to reflux. When addition is complete, the reaction is heated on a steam bath for one hour. The hot solution is then decanted from the residual zinc into 3 liters of ice water, and the resulting mixture is stirred vigorously until the oil solidifies. The mixture is then allowed to stand for 1.5 hours, and the solid is filtered. The solid is washed with water, dried in vacuo and recrystallized to give 21.5 g (31%) of ethyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetate, M.P. 131°- 132°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04440779
Source datasetuspto-grants-1984_04
ORD IDord-505488170c2b4d528249f20b4bfb6f2c
Source noteuspto-grants-1984_04