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Diisopropylamine → 7-Chloro-2-vinylquinoline

HRID 1227124
Notes
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Reaction equation

HRID 1227124 reaction equation
[CH2:1]([Li:2])[CH2:3][CH2:4][CH3:5].[CH3:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].[CH:12]([NH:13][CH:14]([CH3:15])[CH3:16])([CH3:17])[CH3:18].[CH:40]([N-:41][CH:42]([CH3:43])[CH3:44])([CH3:45])[CH3:46].[Cl:19][c:20]1[cH:21][cH:22][c:23]2[cH:24][cH:25][c:26]([CH3:30])[n:27][c:28]2[cH:29]1.[Li+:47].[O:48]1[CH2:49][CH2:50][CH2:51][CH2:52]1.[P:31]([Cl:32])([O:33][CH2:34][CH3:35])([O:36][CH2:37][CH3:38])=[O:39]>>[CH2:1]=[CH:30][c:26]1[cH:25][cH:24][c:23]2[cH:22][cH:21][c:20]([Cl:19])[cH:29][c:28]2[n:27]1
ParticipantsSources & evidenceReaction notes

Participants

9

Reactant 8

HCID 7912DiisopropylamineHCID 8028TetrahydrofuranHCID 8058HexaneHCID 13139Diethyl chlorophosphateHCID 28486Lithium ionHCID 1383957-Chloro-2-methylquinolineHCID 5062348Diisopropylamide
On this pageParticipantsSources & evidenceReaction notes
HCID 178418339
Butyllithium

Product 1

HCID 107028207-Chloro-2-vinylquinoline

Sources & evidence

ORD record
ord-dfea77d86c794d3aa28b0adba93118fa
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI
10.1039/C8SC04228D

Reaction notes

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