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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380129Generated: November 1, 2026

Hydrochloric Acid → HCID 53987327, compound

https://huagongshe.com/reaction/1380129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantDiisopropylamineHCID 7912—
Reactant4-(4-Methoxyphenyl)butyric acidHCID 78280—
ReactantLithiumHCID 3028194—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 53987327HCID 53987327—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of lithium diisiopropylamide (prepared from diisopropylamine (16.16 g, 0.16 mol and n-butyl lithium (1.6M in hexane, 100 ml, 0.016 mol) in THF (50 ml) at -78° C., was added a solution of 4-(4-methoxyphenyl)butanoic acid (13.80 g, 0.07 mol) in THF (100 ml) over 20 min. The solution was warmed to -20° C. and stirred for 2.5 h. Formaldehyde gas generated by warming paraformaldehyde (10 g) was then passed into the reaction mixture in a stream of nitrogen. After stirring for a further 2 h. at -20° C., hydrochloric acid (2N, 500 ml) was added and the reaction mixture was diluted with ethyl acetate (800 ml). After washing with water, the organic phase was extracted with sodium hydroxide solution (0.5N, 3×200 ml). The combined aqueous extracts were acidified with hydrochloric acid and extracted with ethyl acetate (3×200 ml), the combined organic phase (MgSO4) was dried and solvent removed at reduced pressure to give the product as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579862
Source datasetuspto-grants-1986_04
ORD IDord-5fc9290d0f0d4748bb107fcdbe5c0d35
Source noteuspto-grants-1986_04