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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093798Generated: November 1, 2026

Monomethyl terephthalate → Methyl 4-(pyrrolidine-1-carbonyl)benzoate

https://huagongshe.com/reaction/1093798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMonomethyl terephthalateHCID 15513—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantPyrrolidineHCID 31268—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-(pyrrolidine-1-carbonyl)benzoateHCID 1717821081.9%

Reaction Steps

DIPEA (1.26 g, 9.7 mmol) was added to a stirred solution of terephthalic acid monomethyl ester (500 mg, 2.77 mmol) in DMF (3 mL) followed by HOBt (410 mg, 3.0 mmol) and EDCI (1.32 g, 7.0 mmol). After 2 minutes of stirring, pyrrolidine (215 mg, 3.0 mmol) was added and the resulting mixture was stirred at room temperature overnight. The reaction mixture was diluted with cold water, the precipitate was collected to afford 53 mg (81.9% Yield) of 4-(pyrrolidine-1-carbonyl)-benzoic acid methyl ester. LiOH.H2O (285 mg, 6.8 mmol) was added to a solution of 4-(pyrrolidine-1-carbonyl)-benzoic acid methyl ester (530 mg, 2.27 mmol) in a mixture of methanol (2 mL), THF (6 mL) and H2O (2 mL). The reaction mixture was stirred at ambient temperature for 3 hrs. The reaction mixture was concentrated, the residue was diluted with water, and acidified with conc. HCl. The solid was filtered and dried to afford 41 mg (82.32% Yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129376B2
Source datasetuspto-grants-2012_03
ORD IDord-40a1f3062e574f39a4f6700f1f96486f
Source noteuspto-grants-2012_03