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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924342Generated: October 30, 2026

Formaldehyde → HCID 53312154, compound

https://huagongshe.com/reaction/924342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86673650HCID 86673650—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53312154HCID 53312154—

Reaction Conditions

Temperature40 °C

Reaction Steps

(S)-3-Benzoyl-5-biphenyl-4-ylmethyl-1-((E)-styryl)-pyrrolidin-2-one (4a, R1=styryl, R4=phenyl) (1.0 g, 2.2 mmol) is dissolved in 5 mL of anhydrous tetrahydrofuran, add 37% formaldehyde aqueous solution (0.36 mL, 4.4 mmol), 1 M K2CO3 aqueous solution (4.4 mL, 4.4 mmol) and n-Bu4NOH (12 mg, 0.05 mmol), heat to 40° C. for 2 h. The reaction mixture is cooled to room temperature, extract with ethyl acetate, the extracts are washed with saturated Na2CO3 aqueous solution and brine, dry over anhydrous Na2SO4 and concentrate under vacuum, the residue is purified by column chromatography to obtain (R)-5-Biphenyl-4-ylmethyl-3-methylene-1-((E)-styryl)-pyrrolidin-2-one (1a, R1=styryl). Spectroscopic data as Example 23, Method 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278908B2
Source datasetuspto-grants-2016_03
ORD IDord-6ae1b668961443ff8b74b6be8025c1fe
Source noteuspto-grants-2016_03