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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672137Generated: October 31, 2026

Water → 3-(1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl)-2,2-difluoropropanoic acid

https://huagongshe.com/reaction/1672137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhthalic AnhydrideHCID 6811—
ReactantTriethylamineHCID 8471—
Reactant3-Amino-2,2-difluoropropanoic acidHCID 2756405—
SolventTolueneHCID 1140—
Product3-(1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl)-2,2-difluoropropanoic acidHCID 5915833395.1%

Reaction Steps

A suspension of 2,2-difluoro-3-aminopropionic acid A1 (7.08 g, 56.6 mmol) in 250 ml of toluene was treated with phthalic anhydride (8.80 g, 59.4 mmol) and triethylamine (20 mL, 14.35 g, 14.4 mmol) and refluxed with water removed by a Dean-Stark trap, drained 5 times at intervals. After cooling to ambient temperature the solvent was removed in vacuo at 30° C. The residue obtained was partitioned between ethyl acetate and ˜2N HCl (aq) with the aqueous phase extracted a second time with ethyl acetate. Evaporation at 30° C. (in vacuo) of the combined organic phases that had been washed with ˜2N HCl, brine and dried (Na2SO4) afforded 3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2,2-difluoro-propionic acid (13.74 g) A2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998950B2
Source datasetuspto-grants-2011_08
ORD IDord-babdaef1b7e34c8ca458a79625be3f03
Source noteuspto-grants-2011_08