HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638392Generated: October 25, 2026
Potassium Carbonate → 9-Tetradecenyl formate
https://huagongshe.com/reaction/638392
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 9-Tetradecen-1-ol, acetate | HCID 28016 | — |
| Reactant | 9-Decenyl formate | HCID 22223454 | — |
| Reactant | Tetradec-1-enyl formate | HCID 53971419 | — |
| Reactant | Tetradecen-1-ol acetate | HCID 54348667 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 9-Tetradecenyl formate | HCID 92065 | — |
Reaction Steps
Three fields of cotton in a late fruiting stage were used to evaluate the effectiveness of tetradecenyl formate in controlling Heliothis species. In this case, the 9-tetradecenyl formate was prepared from 9-tetradecenyl acetate rather than directly from 9-decenyl formate. In a typical process 21.1 g (0.08 mol) of tetradecenyl acetate, 22.2 g (0.16 mol) K2CO3, 200 mL methanol, and 2 mL water were added to a 500 mL one neck round bottom flask. The mixture was stirred for two hours at room temperature. Then 200 mL of diethyl ether was added, and the mixture was filtered. The ether layer was washed with water, then saturated NaCl solution, then dried over MgSO4. The dried solution was filtered and concentrated on a rotary evaporator. The product consisting of 9-tetradecenyl alcohol was then reacted with formic acid in benzene at gentle reflux (~80° C.) for 24 hours. Then additional formic acid was added and the gentle reflux continued for another 24 hours. The 9 -tetradecenyl formate was recovered by extraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04560792 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-7c65ce5d94404e9e8c86c8b8e94d6dee |
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| Source note | uspto-grants-1985_12 |
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