HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Benzene, 1-bromo-3-(trifluoromethyl)- → 1-Benzhydryl-2-(m-trifluoromethylbenzimidoyl)azetidine

HRID 46456
Notes
Print preview

Reaction equation

HRID 46456 reaction equation
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:4]=[C:5]([Mg]Br)[CH:6]=[CH:7][CH:8]=1.BrC1C=C(C(F)(F)F)C=CC=1.[Mg].[CH:25]([N:38]1[CH2:41][CH2:40][CH:39]1[C:42]#[N:43])([C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>CCOCC>[CH:25]([N:38]1[CH2:41][CH2:40][CH:39]1[C:42](=[NH:43])[C:5]1[CH:6]=[CH:7][CH:8]=[C:3]([C:2]([F:12])([F:11])[F:1])[CH:4]=1)([C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 9817Benzene, 1-bromo-3-(trifluoromethyl)-HCID 5462224MagnesiumHCID 197720721-Benzhydrylazetidine-2-carbonitrileHCID 178506173HCID 178506173, compound

Product 1

HCID 203870491-Benzhydryl-2-(m-trifluoromethylbenzimidoyl)azetidine

Reagents, catalysts & solvents 1

HCID 3283
Diethyl Ether
Solvent
3×

Procedure

Suspend m-trifluoromethylphenylmagnesium bromide in ether by adding a solution of 18 g of m-bromobenzotrifluoride in 30 ml of ether to a stirred suspension of 1.94 g of magnesium turnings in 20 ml of dry ether. Upon completion of addition, allow the reaction mixture to cool to room temperature and add 7.95 g of 1-benzhydryl-2-cyanoazetidine.

Workup

  1. additionUpon completion of addition

Sources & evidence

ORD record
ord-b96407d1931e4a2990162b28f74a60da
Source dataset
uspto-grants-1979_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04173566

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes