Acetonitrile → 2-[6-[(6-Bromohexyl)oxy]-1-hexynyl]quinoline

HRID 671255

Reaction equation

[Br:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][O:19][CH2:20][CH2:21][CH2:22][CH2:23][C:24]#[CH:25].[Br:1][c:2]1[n:3][c:4]2[cH:5][cH:6][cH:7][cH:8][c:9]2[cH:10][cH:11]1.[CH3:39][C:40]#[N:41].[CH:26]1([NH:27][CH:28]2[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33]2)[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38]1.[Cu:42][I:43]>>[c:2]1([C:25]#[C:24][CH2:23][CH2:22][CH2:21][CH2:20][O:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][Br:12])[n:3][c:4]2[cH:5][cH:6][cH:7][cH:8][c:9]2[cH:10][cH:11]1

Participants

Reactant 5

HCID 6342Acetonitrile

HCID 7582Dicyclohexylamine

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)

HCID 27627562-Bromoquinoline

HCID 218671586-[(6-Bromohexyl)oxy]-1-hexyne

Product 1

HCID 198767592-[6-[(6-Bromohexyl)oxy]-1-hexynyl]quinoline

Sources & evidence

ORD record: ord-440ae9e17e94431fbdc57991cf8db666
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Linked notes

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