Acetate → HCID 68513319, compound

HRID 677528Notes

Reaction equation

HRID 677528 reaction equation
[CH3:45][C:46]1([CH3:47])[C:48]([CH3:49])([CH3:50])[O:51][B:52]([c:53]2[cH:54][n:55][n:56]([C:58](=[O:59])[O:60][C:61]([CH3:62])([CH3:63])[CH3:64])[cH:57]2)[O:65]1.[CH3:96][C:97]#[N:98].[CH:66]1([P:67]([CH:68]2[CH2:69][CH2:70][CH2:71][CH2:72][CH2:73]2)[CH:74]2[CH2:75][CH2:76][CH2:77][CH2:78][CH2:79]2)[CH2:80][CH2:81][CH2:82][CH2:83][CH2:84]1.[Cs+:86].[F-:85].[F:1][c:2]1[cH:3][c:4]([NH:28][C:29](=[O:30])[c:31]2[c:32](=[O:44])[n:33](-[c:37]3[cH:38][cH:39][c:40]([F:43])[cH:41][cH:42]3)[n:34][cH:35][cH:36]2)[cH:5][cH:6][c:7]1[O:8][c:9]1[c:10]2[c:11]([n:12][cH:13][cH:14]1)[n:15]([CH2:19][c:20]1[cH:21][cH:22][c:23]([O:26][CH3:27])[cH:24][cH:25]1)[n:16][c:17]2[I:18].[O-:88][C:89]([CH3:90])=[O:91].[O-:92][C:93]([CH3:94])=[O:95].[Pd+2:87]>>[F:1][c:2]1[cH:3][c:4]([NH:28][C:29](=[O:30])[c:31]2[c:32](=[O:44])[n:33](-[c:37]3[cH:38][cH:39][c:40]([F:43])[cH:41][cH:42]3)[n:34][cH:35][cH:36]2)[cH:5][cH:6][c:7]1[O:8][c:9]1[c:10]2[c:11]([n:12][cH:13][cH:14]1)[n:15]([CH2:19][c:20]1[cH:21][cH:22][c:23]([O:26][CH3:27])[cH:24][cH:25]1)[n:16][c:17]2-[c:53]1[cH:54][n:55][n:56]([C:58](=[O:59])[O:60][C:61]([CH3:62])([CH3:63])[CH3:64])[cH:57]1

Participants

9

Reactant 8

HCID 175Acetate2×HCID 6342AcetonitrileHCID 28179Fluoride IonHCID 75806TricyclohexylphosphineHCID 104967Cesium cationHCID 105144Allyl(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)chloropalladium(II)HCID 16217654tert-butyl 4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylateHCID 68513145HCID 68513145, compound

Product 1

HCID 68513319HCID 68513319, compound

Sources & evidence

ORD record
ord-1856aa80aa9f4b00a3baf9ec94478dd7
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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