Ammonia → HCID 67717348, compound

HRID 1451072Notes

Reaction equation

HRID 1451072 reaction equation
[C:1]([CH2:3][C:4]1[CH:5]=[C:6]([CH:11]=[CH:12][CH:13]=1)[C:7]([O:9][CH3:10])=[O:8])#[N:2].CCO.[ClH:17].[NH3:18]>C(Cl)Cl.CO>[ClH:17].[NH2:18][N:2]=[CH:1][CH2:3][C:4]1[CH:5]=[C:6]([CH:11]=[CH:12][CH:13]=1)[C:7]([O:9][CH3:10])=[O:8]

Participants

7

Conditions

Temperature
0 °C

Procedure

A sample of methyl 3-(cyanomethyl)benzoate (1.87 g, 0.011 mol) was dissolved in anhydrous CH2Cl2 (100 mL) containing absolute EtOH (15 mL). The mixture was cooled to 0° C. and a stream of HCl gas passed through the solution for 10 min. The mixture was then refrigerated for 6 days. The mixture was transferred to a 500-mL flask and concentrated in vacuo (0.05 mm Hg) at 0° C. to give a white solid. The solid material was dissolved in anhydrous methanol (200 mL) and anhydrous ammonia passed through the solution for 20 min. The mixture was warmed to 50° C. for 18 h. The solution was cooled and filtered to remove solids. The filtrate was concentrated at room temperature in vacuo to give a white foam (2.5 g, quantitative). A portion (ca. 1 g) of the material was dried over toluene to give methyl 3-[(aminoiminomethyl)methyl]benzoate hydrochloride, mp 139°-140° C.

Workup

  1. customThe mixture was transferred to a 500-mL flask
  2. concentrationconcentrated in vacuo (0.05 mm Hg) at 0° C.
  3. customto give a white solid
  4. temperatureThe mixture was warmed to 50° C. for 18 h
  5. temperatureThe solution was cooled
  6. filtrationfiltered
  7. customto remove solids
  8. concentrationThe filtrate was concentrated at room temperature in vacuo
  9. customto give a white foam (2.5 g, quantitative)
  10. dry with materialA portion (ca. 1 g) of the material was dried over toluene

Sources & evidence

ORD record
ord-844f89b84d914e93947699ca94e32014
Source dataset
uspto-grants-1997_02
Patent number
US05602277

Reaction notes

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