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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602725Generated: November 2, 2026

Trifluoroacetic acid → HCID 19610515, compound

https://huagongshe.com/reaction/1602725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70055592HCID 70055592—
SolventDichloromethaneHCID 6344—
SolventAnisoleHCID 7519—
ProductHCID 19610515HCID 19610515—

Reaction Steps

To a stirred suspension of the product of step (a) (2.9 g) in a mixture of dichloromethane (20 ml) and anisole (2 ml) at 0-5° C. was added trifluoroacetic acid (27 ml). The resultant solution was stirred at low temperature for 20 minutes and then at ambient temperature for 2.5 hours. The reaction mixture was evaporated and the residue was triturated with dry ether. The solid was collected and washed with ether to give methyl 4-(3-methylcarbazoyl)-phenoxyacetate trifluoroacetate salt (2.9 g), as a white solid; m.p. 121-123° C.; NMR Spectrum (DMSO-d6) 2.80 (3H, s), 3.70 (3H, s), 4.93 (2H, s), 7.10 (2H, d), 7.85 (2H, d), 10.80-11.70 (1H, br s); Mass Spectrum m/Z 239 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981531
Source datasetuspto-grants-1999_11
ORD IDord-580336d1c18b4ecbb994a3d66ebb7ab1
Source noteuspto-grants-1999_11