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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706354Generated: October 31, 2026

Trifluoroacetic acid → HCID 86605018, compound

https://huagongshe.com/reaction/706354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58046556HCID 58046556—
SolventDichloromethaneHCID 6344—
ProductHCID 86605018HCID 8660501896%

Reaction Steps

Trifluoroacetic acid (30 ml) was added to a solution of solution of 1-(2-chloropyridin-4-yl)carbonylspiro[indoline-3,4′-piperidine]-1′-carboxylic acid tert-butyl ester (2.3 g) in anhydrous dichloromethane (50 ml), the solution darkening upon addition. The reaction was left as such for 15 min. The reaction mixture was evaporated in vacuo and the dark residue re-suspended in dry ether (100 ml). The residue was triturated until it became a free-flowing beige precipitate. The precipitate was collected by filtration and dried in a stream of nitrogen to give 2.28 g (96%) of the desired amine salt. M.p. 245° C. (decomposition). 1H NMR (400 MHz, d6-DMSO) 1.8 (m, 2H), 1.9 (m, 2H), 2.9 (m, 2H), 3.25 (m, 2H), 3.98 (s, 2H), 7.15-7.3 (m, 2H), 7.24 (d, J=8 Hz, 1H), 7.56 (d, J=7 Hz, 1H), 7.62 (s, 1H), 8.1 (br s, 1H), 8.56 (d, J=7 Hz, 1H), 8.8 (br s, 2H). MS (ES+) 328/330 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174987B2
Source datasetuspto-grants-2015_11
ORD IDord-bd2d9cb2c12b44fa81eed288040e9763
Source noteuspto-grants-2015_11