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1-Fluoro-2,4,6-trimethylpyridinium Tetrafluoroborate (Fluorinating Reagent) → HCID 178475909, compound

HRID 2027696
Notes
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Reaction equation

HRID 2027696 reaction equation
[CH3:1][C:2]([O:4][CH2:5][C@:6]1([C@H:15]([C@@H:9]2[C@H:8]([N:16]3[C:25](=[O:26])[c:24]([c:19]4[C:17]3=[O:18])[cH:23][cH:22][cH:21][cH:20]4)[CH2:7]1)[O:14][C:11]([CH3:13])([CH3:12])[O:10]2)O)=[O:3].Cc1cc(C)[n+]([F:27])c(C)c1.F[B-](F)(F)F>>[CH3:1][C:2]([O:4][CH2:5][C@@:6]1([C@H:15]([C@@H:9]2[C@H:8]([N:16]3[C:25](=[O:26])[c:24]([c:19]4[C:17]3=[O:18])[cH:23][cH:22][cH:21][cH:20]4)[CH2:7]1)[O:14][C:11]([CH3:13])([CH3:12])[O:10]2)[F:27])=[O:3]
ParticipantsConditionsSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 27793091-Fluoro-2,4,6-trimethylpyridinium Tetrafluoroborate (Fluorinating Reagent)HCID 178475954HCID 178475954, compound

Product 1

HCID 178475909HCID 178475909, compound

Reagents, catalysts & solvents 2

HCID 6344DichloromethaneSolventHCID 117669-PhenylanthraceneInternal standard
On this pageParticipantsConditionsSources & evidenceReaction notes

Conditions

Temperature
25 °C

Sources & evidence

ORD record
ord-cb1e152981194debbefbfc459626cea4
Source dataset
39k HTE dataset from Pfizer
DOI
10.1038/s41557
Original link
View source

Reaction notes

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