HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109431Generated: October 26, 2026
1,1,1-Trifluoro-2-octyl p-nitrobenzoate → 1,1,1-Trifluoro-2-octyl p-aminobenzoate
https://huagongshe.com/reaction/1109431
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1,1-Trifluoro-2-octyl p-nitrobenzoate | HCID 15219530 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,1,1-Trifluoro-2-octyl p-aminobenzoate | HCID 15219531 | — |
Reaction Steps
The reaction liquid was poured into water, and extracted with methylene chloride. The methylene chloride layer was washed with a diluted hydrochloric acid and water in this order. The organic layer thus recovered was distilled under a reduced pressure to remove the solvent, and subjected to purification by a silica gel chromatography (n-hexane:ethyl acetate=10:2) to obtain 1.9 g of p-nitrobenzoic acid 1,1,1-trifluoro-2-octyl ester. The ester was dissolved in 30 ml of ethanol, to which 0.19 g of 5% Pd-C catalyst was added. After the solution was stirred overnight under hydrogen atmosphere, the Pd-C catalyst was separated by filtration, and the ethanol was distilled off under a reduced pressure to obtain 1.8 g of p-aminobenzoic acid 1,1,1-trifluoro-2-octyl ester which was the desired compound of the reaction 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05320776 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-bcb78b293cda45cdbd2c89a5ecab4bae |
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| Source note | uspto-grants-1994_06 |
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