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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678616Generated: October 31, 2026

Cyclohexanone → 2-Cyclohexyl-3-oxo-3-(2-oxo-cyclohexyl)-propionic acid ethyl ester

https://huagongshe.com/reaction/1678616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantLithium diisopropylamideHCID 2724682—
Reactantethyl 3-(1H-benzotriazol-1-yl)-2-cyclohexyl-3-oxopropanoateHCID 3722282—
SolventTetrahydrofuranHCID 8028—
Product2-Cyclohexyl-3-oxo-3-(2-oxo-cyclohexyl)-propionic acid ethyl esterHCID 6713123921%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a −78° C. cold solution of LDA (2 M solution in heptane/ethylbenzene/THF, 1.8 ml, 3.66 mmol) in THF (16.8 ml) under an argon atmosphere was added a solution of cyclohexanone (380 μl, 3.66 mmol; CAS Reg. No. 108-94-1) in THF (12.6 ml) within 10 min. The mixture was stirred for 1 h at −78° C. A solution of 3-benzotriazol-1-yl-2-cyclohexyl-3-oxo-propionic acid ethyl ester (1.05 g, 3.33 mmol) in THF (11.1 ml) was added and the solution was stirred at ambient temperature for 14 h. Ice water was added, the mixture was poured onto ice water/brine 1/1 and extracted two times with TBME. The combined extracts were washed with ice water/brine 1/1 and dried over Na2SO4. After filtration the solvent was removed under reduced pressure to give a yellow oil which was purified by column chromatography (silica gel, iPrOAc/heptane) to give the title compound (209 mg, 0.71 mmol; 21%) as yellow oil. MS: m/e=295.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008505B2
Source datasetuspto-grants-2011_08
ORD IDord-9080364217704693a77758b21eb0c23a
Source noteuspto-grants-2011_08