HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102941Generated: October 30, 2026
3,3,3-Trifluoropropyne → HCID 57804176, compound
https://huagongshe.com/reaction/2102941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,3,3-Trifluoropropyne | HCID 69578 | — |
| Reactant | 4-Iodo-3-methylbenzoic acid | HCID 1517322 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57804176 | HCID 57804176 | — |
Reaction Steps
The method is based upon a procedure detailed by Yoneda et al in Bulletin Chemical Society Japan 1990, 63, 2124-2126. A solution of n-butyl lithium (2.5M in hexanes; 1 eq) was added carefully to a solution of 3,3,3-trifluoroprop-1-yne (1 eq) in THF at −78° C. under nitrogen. The mixture was stirred at −78° C. for 30 min then a solution of ZnCl2 (3 eq) in THF was added slowly. The mixture was allowed to warm to room temperature, stirred for 30 min then Pd(Ph3P)4 (5 mol %) was added, followed by 4-iodo-3-methylbenzoic acid (0.5 eq). The mixture was heated to 50° C. and stirred for 15 h, then heated further to 80° C. for 5 h, and finally at 100° C. overnight. After allowing to cool to room temperature the mixture was concentrated under vacuum to a crude residue. The residue was purified by column chromatography on silica gel to give the product as a solid. m/z=227 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576099B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-be95da783e744b6e8fbc1ca100a1bdff |
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| Source note | uspto-grants-2009_08 |
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