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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683251Generated: October 26, 2026

Tetrahydrofuran → trans-2-(4-Hydroxycyclohexyl)-isoindole-1,3-dione

https://huagongshe.com/reaction/1683251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantN-CarbethoxyphthalimideHCID 31187—
ReactantSodium BicarbonateHCID 516892—
Reactant(1s,4s)-4-Aminocyclohexan-1-ol hydrochlorideHCID 522619—
SolventWaterHCID 962—
Producttrans-2-(4-Hydroxycyclohexyl)-isoindole-1,3-dioneHCID 28872672.4%

Reaction Steps

A solution of 4-aminocyclohexanol hydrochloride (6.08 g, 0.04 mole) in water (60 ml) was brought to pH 8 with aqueous sodium bicarbonate solution. N-carbethoxy-phthalimide (8.76 g, 0.04 mole) was added followed by tetrahydrofuran (until homogenous solution was obtained). The clear solution was stirred at room temperature overnight. During this time a white solid was precipitated. The tetrahydrofuran was removed in vacuo and the remaining aqueous solution was extracted with ethyl acetate until the solution was clear. The ethyl acetate extracts were combined, washed with water, dried (MgSO4) and concentrated to give 4-phthalimido cyclohexanol as a white solid (7.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637611
Source datasetuspto-grants-1997_06
ORD IDord-bc3e9e8082a245308ac1288598f482cb
Source noteuspto-grants-1997_06