Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179510Generated: October 31, 2026

Methyl Benzoate → HCID 86673650, compound

https://huagongshe.com/reaction/2179510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl BenzoateHCID 7150—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 53311905HCID 53311905—
SolventTolueneHCID 1140—
ProductHCID 86673650HCID 86673650—

Reaction Steps

(S)-5-Biphenyl-4-ylmethyl-1-((E)-styryl)-pyrrolidin-2-one (3a, R1=styryl) (1.00 g, 2.8 mmol) is heated to dissolve in 3 mL of anhydrous toluene under N2, add t-BuOK (0.43 g, 3.7 mmol) in one portion, stir at this temperature for 10 min, then add methyl benzoate dropwise, the reaction mixture reflux overnight, cool to room temperature, quench with saturated NH4Cl aqueous solution, separate the organic phase, extract with toluene (30 mL*3), the combined organic extracts are washed with saturated Na2CO3 aqueous solution and brine, dry over anhydrous Na2SO4 and concentrate under vacuum. The residue is purified by silica gel column chromatography, eluting with 5:1 heptane/ethyl acetate to obtain (S)-3-Benzoyl-5-biphenyl-4-ylmethyl-1-((E)-styryl)-pyrrolidin-2-one (4a, R1=styryl, R4=phenyl), the ratio of (3S,5S) to (3R,5S) is 70:30 as determine by HPLC. Spectroscopic data as Example 8, Method 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067883B2
Source datasetuspto-grants-2015_06
ORD IDord-b823aa219a3b42bb93872c18fc4bda73
Source noteuspto-grants-2015_06