HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35261Generated: October 28, 2026
Diethylamine → N,N-diethyl-5-(1-methyl-1,2,3,4-tetrazol-5-yl)valeramide
https://huagongshe.com/reaction/35261
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 5-(1-Methyl-1,2,3,4-tetrazol-5-yl)valeric acid | HCID 13203401 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N-diethyl-5-(1-methyl-1,2,3,4-tetrazol-5-yl)valeramide | HCID 13142190 | 29.9% |
Reaction Steps
(5-(1-Methyl-1,2,3,4-tetrazol-5-yl)valeric acid (1.8 g) is dissolved in dimethylformamide (50 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, and the mixture is stirred at room temperature for 30 minutes. To the mixture is added dropwise with stirring diethylamine (0.9 g) at rood temperature, and the mixture is stirred for 2 hours. Dimethylformamide is distilled off under reduced pressure, and the residue is purified by column chromatography (Wakogel C-200). After eluting with benzene-chloroform (1:1), the eluate is distilled under reduced pressure to give N,N-diethyl-5-(1-methyl-1,2,3,4-tetrazol-5-yl)valeramide (0.7 g), colorless liquid, b.p. 190°-200° C. (bath temperature)/0.07 mmHg, nD25 =1.4907.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766120 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-918dd0690f82437b87a16fe418e53ad5 |
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| Source note | uspto-grants-1988_08 |
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