Acetate → HCID 57709128, compound

HRID 1141074Notes

Reaction equation

HRID 1141074 reaction equation
[C:104]([O-:105])(=[O:106])[CH3:107].[C:99]([O-:100])(=[O:101])[CH3:102].[CH2:51]([CH3:52])[C:53]([CH2:54][CH3:55])([c:56]1[cH:57][c:58]([CH3:74])[c:59]([C:62]#[C:63][C:64]2([O:69][Si:70]([CH3:71])([CH3:72])[CH3:73])[CH2:65][CH2:66][CH2:67][CH2:68]2)[cH:60][cH:61]1)[c:75]1[cH:76][c:77]([CH3:90])[c:78]([B:81]2[O:82][C:83]([CH3:84])([CH3:85])[C:86]([CH3:87])([CH3:88])[O:89]2)[cH:79][cH:80]1.[CH3:38][O:39][C:40]([CH2:41][c:42]1[c:43]([F:49])[cH:44][c:45]([Cl:48])[cH:46][cH:47]1)=[O:50].[CH3:92][c:93]1[cH:94][cH:95][cH:96][cH:97][cH:98]1.[CH:1]1([P:2]([CH:3]2[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]2)[c:9]2[cH:10][cH:11][cH:12][cH:13][c:14]2-[c:15]2[c:16]([O:17][CH3:18])[cH:19][cH:20][cH:21][c:22]2[O:23][CH3:24])[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29]1.[K+:35].[K+:36].[K+:37].[OH2:91].[P:30]([O-:31])([O-:32])([O-:33])=[O:34].[Pd+2:103]>>[CH3:38][O:39][C:40]([CH2:41][c:42]1[c:43]([F:49])[cH:44][c:45](-[c:78]2[c:77]([CH3:90])[cH:76][c:75]([C:53]([CH2:51][CH3:52])([CH2:54][CH3:55])[c:56]3[cH:57][c:58]([CH3:74])[c:59]([C:62]#[C:63][C:64]4([O:69][Si:70]([CH3:71])([CH3:72])[CH3:73])[CH2:65][CH2:66][CH2:67][CH2:68]4)[cH:60][cH:61]3)[cH:80][cH:79]2)[cH:46][cH:47]1)=[O:50]

Participants

10

Reactant 9

HCID 175Acetate2×HCID 813Potassium Cation3×HCID 962WaterHCID 1061PhosphateHCID 1140TolueneHCID 105144Allyl(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)chloropalladium(II)HCID 112698722-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 57443493Methyl 2-(4-chloro-2-fluorophenyl)acetateHCID 577089762-(4-{1-Ethyl-1-[3-methyl-4-(1-trimethylsilanyloxy-cyclopentylethynyl)-phenyl]-propyl}-2-methyl-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane

Product 1

HCID 57709128HCID 57709128, compound

Sources & evidence

ORD record
ord-0776a467f0334859b96f469c87e40d2a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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