HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109429Generated: October 31, 2026
HCID 53913940, compound → HCID 54427475, compound
https://huagongshe.com/reaction/1109429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 53913940 | HCID 53913940 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54427475 | HCID 54427475 | — |
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 2.1 g of p-nitrobenzoic acid 1,1,1-trifluoro-2-decyl ester. The ester was dissolved in 30 ml of ethanol, to which 0.21 g of 5 % Pd-C catalyst was added, and the solution was stirred overnight under hydrogen atmosphere, then the Pd-C catalyst was separated by filtration, and the ethanol was distilled off under a reduced pressure to obtain 2.0 g of p-amino-benzoic acid 1,1,1-trifluoro-2-decyl 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-199757cb80f247d496050b288ce926e1 |
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| Source note | uspto-grants-1994_06 |
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