HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156260Generated: November 4, 2026
Trifluoroacetic anhydride → HCID 54574519, compound
https://huagongshe.com/reaction/1156260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3,7,11-Trimethyldodecanoic acid | HCID 192736 | — |
| Reactant | HCID 53820327 | HCID 53820327 | — |
| Catalyst | Perchloric Acid | HCID 24247 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54574519 | HCID 54574519 | — |
Reaction Steps
A mixture of 24.2 g (0.1 mole) of 3,7,11-trimethyldodecanoic acid and 21.0 g (0.1 mole) of trifluoroacetic anhydride is stirred at reflux for 1/2 hour. The mixture is cooled and 18.0 g (0.1 mole) of ethyl 3-(2-furanyl)-2-methylpropenoate is added. The mixture is cooled to about 0° C. and 5 drops of 70% perchloric acid is added. The mixture is stirred at 0° C. for 2 hours, then diluted with anhydrous ether and treated with saturated aqueous sodium carbonate solution until basic. The layers are separated and the ether layer washed with water, brine and evaporated to dryness. The residue is distilled at reduced pressure to give ethyl 2-methyl-3-[5-(1-oxo-3,-7,11-trimethyldodecyl)-2-furanyl]-2-propenoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04335098 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-50551235ea1c42aead934b1e34fdabc7 |
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| Source note | uspto-grants-1982_06 |
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