Carbon Dioxide → HCID 66854287, compound

HRID 1211994Notes

Reaction equation

HRID 1211994 reaction equation
[CH2:33]([c:34]1[cH:35][cH:36][cH:37][cH:38][cH:39]1)[CH3:40].[CH3:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH3:52].[CH:22]([N-:23][CH:24]([CH3:25])[CH3:26])([CH3:27])[CH3:28].[Cl:1][c:2]1[c:3](-[n:8]2[n:9][c:10]([C:13]([F:14])([F:15])[F:16])[n:11][cH:12]2)[n:4][cH:5][cH:6][cH:7]1.[Li+:29].[O:17]1[CH2:18][CH2:19][CH2:20][CH2:21]1.[O:30]=[C:31]=[O:32].[O:41]1[CH2:42][CH2:43][CH2:44][CH2:45]1>>[Cl:1][c:2]1[c:3](-[n:8]2[n:9][c:10]([C:13]([F:14])([F:15])[F:16])[n:11][c:12]2[C:31](=[O:30])[OH:32])[n:4][cH:5][cH:6][cH:7]1

Participants

8

Reactant 7

HCID 280Carbon DioxideHCID 7500EthylbenzeneHCID 8028Tetrahydrofuran2×HCID 8900HeptaneHCID 28486Lithium ionHCID 5062348DiisopropylamideHCID 668546483-chloro-2-(3-trifluoromethyl-1H-1,2,4-triazol-1-yl)pyridine

Product 1

HCID 66854287HCID 66854287, compound

Sources & evidence

ORD record
ord-c233277f7a2247cca6b4664d1f80451b
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)

Reaction notes

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