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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | ethyl 3-(1H-benzotriazol-1-yl)-2-cyclohexyl-3-oxopropanoate | HCID 3722282 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Cyclohexyl-3-oxo-3-(2-oxo-cyclohexyl)-propionic acid ethyl ester | HCID 67131239 | 21% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008505B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-9080364217704693a77758b21eb0c23a |
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| Source note | uspto-grants-2011_08 |
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