Propargyl alcohol → HCID 69099881, compound

HRID 2133351Notes

Reaction equation

HRID 2133351 reaction equation
[Br:1][c:2]1[cH:3][cH:4][c:5]([N:8]([CH2:9][CH2:10][c:11]2[cH:12][cH:13][c:14]([O:15][C:16]([C:17](=[O:18])[O:19][CH2:20][CH3:21])([CH3:22])[CH3:23])[cH:24][cH:25]2)[CH2:26][c:27]2[cH:28][cH:29][c:30]([O:33][C:34]([F:35])([F:36])[F:37])[cH:31][cH:32]2)[n:6][cH:7]1.[CH2:38]([C:39]#[CH:40])[OH:41].[CH3:42][CH2:43][N:44]([CH2:45][CH3:46])[CH2:47][CH3:48].[Cu:126][I:127].[cH:49]1[cH:50][cH:51][c:52]([P:53]([Pd:54]([P:55]([c:56]2[cH:57][cH:58][cH:59][cH:60][cH:61]2)([c:62]2[cH:63][cH:64][cH:65][cH:66][cH:67]2)[c:68]2[cH:69][cH:70][cH:71][cH:72][cH:73]2)([P:74]([c:75]2[cH:76][cH:77][cH:78][cH:79][cH:80]2)([c:81]2[cH:82][cH:83][cH:84][cH:85][cH:86]2)[c:87]2[cH:88][cH:89][cH:90][cH:91][cH:92]2)[P:93]([c:94]2[cH:95][cH:96][cH:97][cH:98][cH:99]2)([c:100]2[cH:101][cH:102][cH:103][cH:104][cH:105]2)[c:106]2[cH:107][cH:108][cH:109][cH:110][cH:111]2)([c:112]2[cH:113][cH:114][cH:115][cH:116][cH:117]2)[c:118]2[cH:119][cH:120][cH:121][cH:122][cH:123]2)[cH:124][cH:125]1>>[c:2]1([C:40]#[C:39][CH2:38][OH:41])[cH:3][cH:4][c:5]([N:8]([CH2:9][CH2:10][c:11]2[cH:12][cH:13][c:14]([O:15][C:16]([C:17](=[O:18])[O:19][CH2:20][CH3:21])([CH3:22])[CH3:23])[cH:24][cH:25]2)[CH2:26][c:27]2[cH:28][cH:29][c:30]([O:33][C:34]([F:35])([F:36])[F:37])[cH:31][cH:32]2)[n:6][cH:7]1

Participants

6

Reactant 5

HCID 7859Propargyl alcoholHCID 8471TriethylamineHCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 59643326HCID 59643326, compoundHCID 178420554HCID 178420554, compound

Product 1

HCID 69099881HCID 69099881, compound

Sources & evidence

ORD record
ord-2c8c319b0707475f87673fed9ce6a394
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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