Ammonia → 4-[(3-Amino-2-hydroxypropyl)oxy]benzonitrile

HRID 1596435Notes

Reaction equation

HRID 1596435 reaction equation
CC(O)C.[O:5]1[CH2:7][CH:6]1[CH2:8][O:9][C:10]1[CH:17]=[CH:16][C:13]([C:14]#[N:15])=[CH:12][CH:11]=1.[NH3:18]>>[C:14]([C:13]1[CH:16]=[CH:17][C:10]([O:9][CH2:8][CH:6]([OH:5])[CH2:7][NH2:18])=[CH:11][CH:12]=1)#[N:15]

Participants

4

Procedure

IPA (300 mL) was added to a stirred suspension of 4-(2-oxiranylmethoxy)benzonitrile (100 g; 571 mmol; see Example A above) in NH3 (500 mL; conc.), and the reaction mixture was stirred at rt. for 3 days. The precipitate was filtered off and the residue concentrated and recrystallized from MeCN to give the sub-title compound in a 46% yield.

Workup

  1. filtrationThe precipitate was filtered off
  2. concentrationthe residue concentrated
  3. customrecrystallized from MeCN

Sources & evidence

ORD record
ord-59d8ec3884e7443da972ec7c6e9e3b19
Source dataset
uspto-grants-2001_09
Patent number
US06291475B1

Reaction notes

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