Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284553Generated: October 30, 2026

Water → 2-phenyl-2-(1H-pyrrol-1-yl)acetic acid

https://huagongshe.com/reaction/1284553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-PhenylglycineHCID 3866—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
SolventDimethylformamideHCID 6228—
Product2-phenyl-2-(1H-pyrrol-1-yl)acetic acidHCID 2741447—

Reaction Steps

15.1 g (0.1 mole) of alpha-phenylglycine were resuspended in 450 ml of dimethylformamide, followed by the addition of 15 g of p-toluene sulphonic acid and 13.2 g (0.1 mole) of 2,5-dimethoxytetrahydrofuran. The mixture was heated to boiling, and at about 95° C. all the solid product was dissolved, the boiling temperature being held for about 60 minutes. After this time, the mixture was cooled, 400 ml of cold water were added and the total mixture was cooled to between 0°-5° C. The mixture was extracted twice with 200 ml of ethyl ether each time, the ether phases being discarded. The aqueous phase was extracted with 500 ml chloroform at pH 1.5. The chloroform extract was treated with 600 ml water and the pH was adjusted to 11. After separating the phases, 500 ml of chloroform were added to the aqueous extract, the pH being adjusted to 1.5 with 2N HCl. The chloroform phase was concentrated to obtain an oil which was crystallised from methanol-water. After drying, the alpha-(N-pyrrolyl)-phenylacetic acid obtained weighed 5.8 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563477
Source datasetuspto-grants-1986_01
ORD IDord-e2c05f97a6bf4ce7bebed9d7aea90bce
Source noteuspto-grants-1986_01