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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048400Generated: November 1, 2026

(S)-5-((3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-2-oxopiperidin-1-yl)heptanal → HCID 67999566, compound

https://huagongshe.com/reaction/1048400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-5-((3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-2-oxopiperidin-1-yl)heptanalHCID 86660731—
ReactantHCID 178418573HCID 178418573—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67999566HCID 67999566—

Reaction Steps

To a solution of (S)-5-((3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-2-oxopiperidin-1-yl)heptanal prepared above in Step A (138 mg, 0.284 mmol) in THF (2.8 mL) was added 1.4 M methylmagnesium bromide in toluene and THF (75:25) (608 μL, 0.851 mmol) at 0° C. Then the reaction was allowed to warm to rt and stirred for 2 h. The reaction was quenched (sat NH4Cl solution), extracted (2×EtOAc), and washed (sat. aq. NaCl solution). The combined organic layer was dried (Na2SO4) and concentrated under reduced pressure to provide the title compound as a colorless film.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-9f6b6c772e6d4a04af2e3176508797fc
Source noteuspto-grants-2013_10