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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284438Generated: October 31, 2026

3,3,3-Trifluoropropyne → HCID 66523230, compound

https://huagongshe.com/reaction/2284438

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3,3-TrifluoropropyneHCID 69578—
Reactant4-((Benzyloxy)carbonyl)piperazine-2-carboxylic acidHCID 5058362—
ReactantHCID 117678427HCID 117678427—
SolventO-XyleneHCID 7237—
ProductHCID 66523230HCID 6652323061%

Reaction Conditions

Temperature-78 °C

Reaction Steps

5-[(Benzyloxy)carbonyl]-4,5,6,7-tetrahydro[1,2,3]oxadiazolo[3,4-a]pyrazin-8-ium-3-olate (C58, prepared from 4-[(benzyloxy)carbonyl]piperazine-2-carboxylic acid using the general procedure described by T. S. Mansour et al., 2006, PCT Intl. Appl. WO 2006/130588) (65 g, 0.24 mol) was dissolved in o-xylene (250 mL) and cooled to −78° C. in a bomb reactor. 3,3,3-Trifluoroprop-1-yne (25 g, 0.27 mol) was injected into the reaction mixture, and the bomb was heated to 270° C. for 24 hours. After cooling to room temperature, the reaction was concentrated in vacuo, and the residue was purified by silica gel chromatography to provide C60 as white crystals. Yield: 7.5 g, 23 mmol, 10%. [The major regioisomer, benzyl 2-(trifluoromethyl)-6,7-dihydropyrazolo[1,5-a]pyrazine-5(4H)-carboxylate (C59), was also isolated, in 61% yield.]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145427B2
Source datasetuspto-grants-2015_09
ORD IDord-c1d5291a2c4b4bffa9e8d0269a50c455
Source noteuspto-grants-2015_09