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Ammonium → 1-Benzhydryl-3-methylazetidine-3-carbonitrile

HRID 1230043
Notes
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Reaction equation

HRID 1230043 reaction equation
[CH3:32][I:33].[CH3:41][CH2:42][CH2:43][CH2:44][CH2:45][CH3:46].[CH3:8][CH2:9][CH2:10][CH2:11][Li:12].[CH:13]([c:14]1[cH:15][cH:16][cH:17][cH:18][cH:19]1)([c:20]1[cH:21][cH:22][cH:23][cH:24][cH:25]1)[N:26]1[CH2:27][CH:28]([C:30]#[N:31])[CH2:29]1.[CH:1]([NH:2][CH:3]([CH3:4])[CH3:5])([CH3:6])[CH3:7].[Cl-:34].[NH4+:35].[O:36]1[CH2:37][CH2:38][CH2:39][CH2:40]1>>[CH3:1][C:28]1([C:30]#[N:31])[CH2:27][N:26]([CH:13]([c:14]2[cH:15][cH:16][cH:17][cH:18][cH:19]2)[c:20]2[cH:21][cH:22][cH:23][cH:24][cH:25]2)[CH2:29]1
ParticipantsSources & evidenceReaction notes

Participants

9

Reactant 8

HCID 223AmmoniumHCID 312ChlorideHCID 6328Methyl iodideHCID 7912DiisopropylamineHCID 8028TetrahydrofuranHCID 8058HexaneHCID 27792901-(Diphenylmethyl)azetidine-3-carbonitrile
HCID 178418339
Butyllithium

Product 1

HCID 100840771-Benzhydryl-3-methylazetidine-3-carbonitrile

Sources & evidence

ORD record
ord-a8670093277e4a3e8ba1af7a3ba2b7c7
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes