Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764772Generated: November 1, 2026

Dimethylformamide → HCID 20331942, compound

https://huagongshe.com/reaction/1764772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
ReactantHCID 178479233HCID 178479233—
SolventAcetoneHCID 180—
ProductHCID 20331942HCID 20331942—

Reaction Steps

To a solution of 22.8 g. (12.5 mmol) of 1-(2-aminoethyl)-1,4-dihydro-5H-tetrazole-5-thione, hydrochloride in 100 ml. of N,N-dimethylformamide and 100 ml. of acetone was added 34.3 ml. (25 mmol) of triethylamine. To the resulting suspension was added slowly a solution of 19.5 g. (12.5 mmol) of p-methoxybenzyl chloride in 30 ml. of acetone. After stirring at room temperature for 15 hours, the mixture was filtered. The filtrate was evaporated to dryness. The residue was taken up in 350 ml. of 5% NaHCO3, and extracted with ethyl acetate. The combined extract was dried (MgSO4) and evaporated to dryness to give an oil which was chromatographed on a silica gel column, eluting with a gradient of 5-10% ethanol in chloroform. Fractions containing product by thin layer chromatography were pooled, and evaporated to dryness to give 1-(2-aminoethyl)-5-(4-methoxybenzylthio)-1H-tetrazole as a brown oil (26 g., 80%). An analytical sample of the crystalline amine hydrochloride (mp 148°-150°) was obtained by treating the product with an ethereal HCl solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04117125
Source datasetuspto-grants-1978_09
ORD IDord-fa3322653aba400696268ff9a5e2ca5d
Source noteuspto-grants-1978_09