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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52865Generated: October 28, 2026

Cyclohexane → Dibenzhydryl carboxymethylsuccinate

https://huagongshe.com/reaction/52865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
ReactantTrityl acetateHCID 621194—
ReactantLithium diisopropylamideHCID 2724682—
ReactantDibenzhydryl maleateHCID 67644151—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductDibenzhydryl carboxymethylsuccinateHCID 1907362629%

Reaction Steps

The reaction product obtained by conducting the Michael-addition reaction in the same manner as in Example 116 using 5.7 ml of a 1.5M cyclohexane solution of lithium diisopropylamide, 2.6 g of trityl acetate and 3.2 g of dibenzhydryl maleate, was dissolved in a liquid mixture of 20 ml of acetic acid and 5 ml of water, and the solution was left to stand at room temperature overnight and then evaporated to dryness under reduced pressure. The residue was subjected to silica gel column chromatography (chloroform/methanol=100/1→10/1) to obtain 1.05 g (yield: 29%) of the above-identified compound as white crystalline powder having a melting point of from 105° to 106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616803
Source datasetuspto-grants-1997_04
ORD IDord-108a59315e044653b584b263eaa291a3
Source noteuspto-grants-1997_04