HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362820Generated: October 31, 2026
Trifluoroacetic acid → (E)-2-(4,6-difluoro-1-indanylidene)acetic acid
https://huagongshe.com/reaction/362820
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-(4,6-Difluoro-1-hydroxy-1-indanyl)acetic acid | HCID 10911298 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-2-(4,6-difluoro-1-indanylidene)acetic acid | HCID 10976722 | 60.9% |
Reaction Steps
Trifluoroacetic acid (39.9 g, 0.35 mol) was added dropwise to a stirred, chilled (ice-methanol bath) mixture of 2-(4,6-difluoro-1-hydroxy-1-indanyl)acetic acid (11.3 g, 0.05 mol) in dichloromethane (250 mL). After 35 min. the mixture was concentrated in vacuo. Dichloromethane was added to the residue and the mixture was concentrated in vacuo. This procedure was repeated once more to give 6.4 g of crude (E)-2-(4,6- difluoro-1-indanylidene) acetic acid. Recrystallization of 0.9 g from acetone: water mixtures gave 0.15 g of (E)-2-(4,6-difluoro-1-indanylidene) acetic acid as a white solid: mp 238°-239° C.; NMR (DMSO-d6): d12.25 (br, 1H), 7.23-7.65 (m, 2H), 6.46 (t, 1H), 3.20-3.28, 2.97-3.20(2 m's, 4H); steady-state nOe: irradiation at 6.46 d, observed 21.6% nOe at 7.63 d.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05872118 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-a1c130c3073d4ec1a9aaa92096667493 |
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| Source note | uspto-grants-1999_02 |
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