Triphenylphosphine → HCID 58235284, compound

HRID 1540688Notes

Reaction equation

HRID 1540688 reaction equation
[Br:1][c:2]1[cH:3][c:4]([NH2:8])[cH:5][n:6][cH:7]1.[C:9](#[CH:10])[Si:11]([CH3:12])([CH3:13])[CH3:14].[Cu:56][I:57].[Pd:15]([Cl:16])[Cl:17].[c:18]1([P:19]([c:20]2[cH:21][cH:22][cH:23][cH:24][cH:25]2)[c:26]2[cH:27][cH:28][cH:29][cH:30][cH:31]2)[cH:32][cH:33][cH:34][cH:35][cH:36]1.[c:37]1([P:38]([c:39]2[cH:40][cH:41][cH:42][cH:43][cH:44]2)[c:45]2[cH:46][cH:47][cH:48][cH:49][cH:50]2)[cH:51][cH:52][cH:53][cH:54][cH:55]1>>[c:2]1([C:10]#[C:9][Si:11]([CH3:12])([CH3:13])[CH3:14])[cH:3][c:4]([NH2:8])[cH:5][n:6][cH:7]1

Participants

6

Reactant 5

HCID 11776Triphenylphosphine2×HCID 24290Palladium ChlorideHCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 66111TrimethylsilylacetyleneHCID 8176813-Amino-5-bromopyridine

Product 1

HCID 58235284HCID 58235284, compound

Sources & evidence

ORD record
ord-1813337664844044b6c304e72ab173cb
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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