N-Methylaniline → Benzamidine

HRID 2287142Notes

Reaction equation

HRID 2287142 reaction equation
C[NH:2][C:3]1C=CC=CC=1.C([Li])CCC.C1C=CC([N:20]=C(Cl)Cl)=CC=1.[CH3:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]>O1CCCC1>[C:3]([NH2:2])(=[NH:20])[C:26]1[CH:25]=[CH:24][CH:29]=[CH:28][CH:27]=1

Participants

6

Conditions

Temperature
0 °C

Procedure

To 2.14 g (0.02 mol) of N-methylaniline in 20 ml of anhydrous tetrahydrofuran at 0° C. under a nitrogen atmosphere was added 8 ml of 2.5 M n-butyl lithium in hexane. The solution was stirred for one hour at 0° C. To the lithium N-methylanilide solution at -23° C. was added 3.48 g (0.02 mol) of phenyl isocyanide dichloride in 5 ml of tetrahydrofuran dropwise. The mixture was stirred for 15 minutes at -23° C. and one hour at 0° C. to afford a clear yellow solution to which 4.8 g (0.04 mol) of benzamidine in 15 ml of tetrahydrofuran was added dropwise. The mixture was stirred for 21 hours at ambient temperature, concentrated and chromatographed on 150 g of silica gel using 1:6 methanol-dichloromethane. The chromatographed product was precipitated by adding a methanolic solution of the product to a large volume of ether and finally recrystallized twice from methanol-ether to afford 1.72 g (24%) of (N-methyl-N,N'-diphenylguanyl)benzimidamide hydrochloride, mp 243°-244° C.

Workup

  1. stirringThe mixture was stirred for 15 minutes at -23° C. and one hour at 0° C.

Sources & evidence

ORD record
ord-ed528e9d915546c2adaa069e47109e19
Source dataset
uspto-grants-1981_05
Patent number
US04269837

Reaction notes

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