HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422179Generated: October 26, 2026
(3-Benzyloxy-5-trifluoromethylthien-2-yl)-carboxylic acid → 3-Benzyloxy-5-trifluoromethylthiophen
https://huagongshe.com/reaction/1422179
Participants
| Role | Name | HCID | Charge |
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| Reactant | (3-Benzyloxy-5-trifluoromethylthien-2-yl)-carboxylic acid | HCID 11426602 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Quinoline | HCID 7047 | — |
| Product | 3-Benzyloxy-5-trifluoromethylthiophen | HCID 11184470 | 71% |
Reaction Steps
A mixture of 1F (14.5 g) and quinoline (50 ml) was treated with copper powder (4.57 g) and heated to 150 ° C. The reaction mixture is heated for 25 minutes at 150° C. and cooled to room temperature. The mixture was filtered and washed with water. Aqueous quinoline was acidified with 6N HCl (pH=2) and extracted with diethyl ether twice. The combined organic phases were washed with water and dried. The mixture was concentrated and the residue was chromatographed to yield a yellow liquid (8.74 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06080861 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-03359913941640338a5dac1b94a9abf9 |
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| Source note | uspto-grants-2000_06 |
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