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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712244Generated: October 29, 2026

Phthalic Anhydride → Ethyl 4-(1,3-dioxoisoindolin-2-yl)cyclohexanecarboxylate

https://huagongshe.com/reaction/712244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-aminocyclohexanecarboxylateHCID 409963—
SolventTolueneHCID 1140—
ProductEthyl 4-(1,3-dioxoisoindolin-2-yl)cyclohexanecarboxylateHCID 408230934.1%

Reaction Steps

A solution of ethyl 4-aminocyclohexanecarboxylate (0.50 g, 2.92 mmol) in toluene (10 mL) was added Et3N (1.02 mL, 7.30 mmol) and phthalic anhydride (0.56 g, 3.80 mmol) and the mixture refluxed for 6-8 h using dean-stark apparatus to remove water. After completion of the reaction (by TLC), the solvent was evaporated under reduced pressure, water (50 mL) added and stirred for 30 min at rt. The solid material thus obtained was collected by filtration under vacuum and dried to obtain the desired product as off-white solid (0.30 g, 34%). 1H NMR (DMSO-d6): δ 7.84 (s, 4H), 4.19 (q, J=7.20 Hz, 2H), 3.71 (m, 1H), 2.71 (m, 1H), 2.06 (m, 2H), 1.90 (m, 2H), 1.69 (m, 2H), 1.60 (m, 2H), and 1.23 (t, J=7.20 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181234B2
Source datasetuspto-grants-2015_11
ORD IDord-581955aa14894ae99c3fa801f20e347b
Source noteuspto-grants-2015_11