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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924341Generated: October 30, 2026

Formaldehyde → HCID 53312154, compound

https://huagongshe.com/reaction/924341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 86673650HCID 86673650—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53312154HCID 53312154—

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 paraformaldehyde (80 mg, 2.6 mmol), DBU (434 mg, 2.8 mmol) and anhydrous Lithium chloride (186 mg, 4.4 mmol), reflux overnight under nitrogen atmosphere. The reaction mixture is cooled to room temperature, add 20 mL of toluene, wash with 5% HCl(aq), saturated Na2CO3 and brine, dry over anhydrous Na2SO4, evaporate the solvent under vacuum to give (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-d4dcfa8f888c446d8ea70587d1cc0b89
Source noteuspto-grants-2016_03