HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35259Generated: October 28, 2026
Diethylamine → HCID 13203396, compound
https://huagongshe.com/reaction/35259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 5-(1-Phenyl-1,2,3,4-tetrazol-5-yl)valeric acid | HCID 14230065 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13203396 | HCID 13203396 | 39.2% |
Reaction Steps
5-(1-Phenyl-1,2,3,4-tetrazol-5-yl)valeric acid (2.5 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 room temperature, and the mixture is stirred for 2 hours. After distilling off dimethylformamide under reduced pressure, acetone is added to the resulting residue, and the insoluble materials are filtered off. The mother liquor is concentrated and then purified by column chromatography (Kieselgel 60, made by Merck & Co.). By eluting with chloroform, there is obtained N,N-diethyl-5-(1-phenyl-1,2,3,4-tetrazol-5-yl)valeramide (1.2 g), colorless liquid, nD25 =1.5303.
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-1fed7466503846a38efc084e4832ca70 |
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| Source note | uspto-grants-1988_08 |
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