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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055785Generated: October 26, 2026

Diisopropylcarbodiimide → 6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-hexanoic Acid Pentafluorophenyl Ester

https://huagongshe.com/reaction/1055785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantPentafluorophenolHCID 13041—
Reactant1,3-Dihydro-1,3-dioxo-2H-isoindole-2-hexanoic acidHCID 78185—
SolventDichloromethaneHCID 6344—
Product6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-hexanoic Acid Pentafluorophenyl EsterHCID 59347289101.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Referring to scheme 12, compound 41a (13.3 g, 51 mmol) was dissolved in anhydrous dichloromethane (40 mL) and cooled to 0° C. under argon. To the solution were added diisopropyl carbodiimide (6.31 g, 7.7 mL, 50 mmol) and pentafluoro phenol (42, 9.2 g, 50 mmol). After overnight the reaction mixture was evaporated to dryness. To the residue ethyl acetate (100 mL) was added and the filtered to remove diisopropyl urea. The precipitate was washed with ethyl acetate (50 mL). The combined organic layer was washed with saturated sodium bicarbonate and water. The organic layer was dried over sodium sulfate, filtered and evaporated to dryness. Compound 43a (Rf=0.8 in 10% EtOAc/Hexane, 21.65 g, 92%) was obtained, which was directly used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394540B2
Source datasetuspto-grants-2016_07
ORD IDord-a7d17c5d571c48af99ee17648c0d0826
Source noteuspto-grants-2016_07