Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Palmitoyl chloride | HCID 8206 | — |
| Reactant | HCID 178506305 | HCID 178506305 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20263705 | HCID 20263705 | 43.7% |
Reaction Steps
6.9 g of 5-trifluoromethyl-1,2,3,4-tetrazole and 13.7 g of palmitoyl chloride were dissolved in 100 ml of acetonitrile while cooling with ice and to the solution was added dropwise 4.5 ml of pyridine over a period of about 10 minutes. After the completion of the dropwise addition, the mixture was stirred at about 5° C. for 30 minutes and then at room temperature for 1 hour, and to the mixture was added dropwise about 100 ml of ice water. The crystals thus-deposited were collected by filtration to obtain 8.2 g of 1-hexadecanoyl-5-trifluoromethyl-1,2,3,4 -tetrazole. A melting point was 66° to 69° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04546075 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-8c5e73afbf9a4faea9e53a36551afd1a |
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| Source note | uspto-grants-1985_10 |
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