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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507689Generated: October 31, 2026

Triethylamine → HCID 89610545, compound

https://huagongshe.com/reaction/1507689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 89610390HCID 89610390—
SolventWaterHCID 962—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductHCID 89610545HCID 8961054583%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of diethyl 3,4-bis(benzyloxy)-1-(4-methoxyphenyl)-1H-pyrrole-2,5-dicarboxylate (1) (39.6 g, 74.8 mmol) in THF/EtOH (300/50 mL) was added NaOH (3.07 g, 77 mmol) as a solution in water (20 mL). The reaction was stirred at 50° C. for 16 h. Triethylamine was added (30 mL, 215 mmol) and the volatiles were removed in vacuo. The residue was purified by silica gel chromatography (50% isohexane:DCM (+2% Et3N), then 20% MeOH/EtOAc (+2% Et3N)) to afford triethylammonium 3,4-bis(benzyloxy)-5-(ethoxycarbonyl)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate (5) (39.3 g, 83%) as a yellow oil: m/z 502 (M+H)+ (ES+); 500 (M−H)− (ES−). 1H NMR (400 MHz, DMSO-d6) δ: 7.51-7.26 (m, 10H), 7.11-7.05 (m, 2H), 6.92-6.83 (m, 2H), 5.09 (s, 2H), 5.06 (s, 2H), 3.95 (q, J=7.1 Hz, 2H), 3.79 (s, 3H), 2.85-2.62 (m, 6H), 1.08-0.92 (m, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221756B2
Source datasetuspto-grants-2015_12
ORD IDord-1d1a5f0a8be3461ab896d5afb2471e6f
Source noteuspto-grants-2015_12