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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35249Generated: October 25, 2026

Diethylamine → N,N-diethyl-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide

https://huagongshe.com/reaction/35249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 178482013HCID 178482013—
SolventTetrahydrofuranHCID 8028—
ProductN,N-diethyl-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramideHCID 2115394854%

Reaction Steps

4-(1-Methyl-1,2,3,4-tetrazol-5-yl)thio-butyric acid (2 g) is dissolved in dry tetrahydrofuran (30 ml), and thereto is added triethylamine (1.1 g). To the mixture is added dropwise with stirring isobutyl chloroformate (1.5 g) under ice-cooling. The mixture is stirred at room temperature for 30 minutes. To the mixture is further added dropwise with stirring diethylamine (0.9 g) at room temperature, and the mixture is stirred for 2 hours. The mixture is concentrated under reduced pressure, and the resulting residue is purified by subjecting it to column chromatography (Kieselgel 60, made by Merck & Co.). By eluting with n-hexaneethyl acetate (1:1), there is obtained N,N-diethyl-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide (1.4 g), colorless liquid, nD17.5 =1.5227.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766120
Source datasetuspto-grants-1988_08
ORD IDord-78fb2885d3ea475e8b0b26aab8d14d29
Source noteuspto-grants-1988_08