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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820923Generated: November 1, 2026

Water → HCID 178501163, compound

https://huagongshe.com/reaction/1820923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
ReactantSodium methanolate methanolHCID 23694274—
ProductHCID 178501163HCID 178501163—

Reaction Steps

Dimethyl trans-cyclohexane-1,4-dicarboxylate (150.0 g) obtained in (1) above is dissolved in tetrahydrofuran (1500 ml), and to the solution is added dropwise a mixed solution of 28% sodium methoxide/methanol (149 g) and water (13.2 g) under ice-cooling. The reaction solution is warmed to room temperature, stirred for 3.5 hours, and thereto is poured n-hexane (1500 ml). The mixture is filtered to collect the precipitates. The resulting solid precipitates are added to a mixture of conc. hydrochloric acid (50 ml), water (450 ml) and chloroform (1000 ml) under ice-cooling, and the mixture is stirred at room temperature for 20 minutes. The chloroform layer is separated and the aqueous layer is extracted with chloroform. The organic layers are combined, dried over sodium sulfate and evaporated to remove the solvent under reduced pressure. The resulting residue is crystallized from n-hexane, collected by filtration and dried to give trans-4-(methoxycarbonyl)cyclohexanecarboxylic acid (106.0 g). ESI-MS M/Z:185[M−H]−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605158B2
Source datasetuspto-grants-2009_10
ORD IDord-9dc8a7ace0f24104ac9f7e7eeb9de45a
Source noteuspto-grants-2009_10