Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954867Generated: November 2, 2026

Trifluoroacetic acid → (E)-2-(4,6-difluoro-1-indanylidene)acetic acid

https://huagongshe.com/reaction/1954867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-(4,6-Difluoro-1-hydroxy-1-indanyl)acetic acidHCID 10911298—
SolventDichloromethaneHCID 6344—
Product(E)-2-(4,6-difluoro-1-indanylidene)acetic acidHCID 1097672260.9%

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 solid white: mp 238-239° C.; NMR (DMSO-d6): d 12.25 (br, 1H), 7.23-7.65 (m, 2H), 6.46 (t, 1H), 3.20-3.28, 2.97-3.20 (2m's, 4H); steady-state nOe: irradiation at 6.46 d, observed 21.6% nOe at 7.63 d.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124284
Source datasetuspto-grants-2000_09
ORD IDord-a6e59663661743b380724392ccb99ece
Source noteuspto-grants-2000_09