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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534534Generated: October 30, 2026

Formaldehyde → HCID 15086755, compound

https://huagongshe.com/reaction/1534534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPiperidineHCID 8082—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Pyrrolidinone, 4-(acetyloxy)-1-(2-propynyl)-, (S)-HCID 15046666—
SolventAcetic AcidHCID 176—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15086755HCID 15086755—

Reaction Steps

A mixture of 1.5 g of (S)-4-(acetyloxy)-1-(2-propynyl)-2-pyrrolidinone, 20 ml of dry dioxane, 1.64 ml of piperidine, 0.66 g of paraformaldehyde, 3.0 ml of acetic acid and 42 mg of cupric chloride was stirred for 30 minutes and then heated at reflux for 45 minutes. The mixture was basified to pH 10 with ammonium hydroxide and then extracted with 5×50 ml of dichloromethane The extracts were combined, dried, filtered and concentrated with toluene in vacuo. The residual oil was chromatographed on deactivated alumina, giving 2.3 g of the desired product as a pale yellow oil [α]D26° =-17° (dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089518
Source datasetuspto-grants-1992_02
ORD IDord-7e4f37f7e7354a82b5e3b53de4b87000
Source noteuspto-grants-1992_02