Ammonia → HCID 15300852, compound
Reaction equation
S(=O)(=O)(O)O.[Cl:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([Cl:13])[C:8]=1[CH:14]([NH:18]C1C(=O)NC=CC=1)[C:15]([NH2:17])=[O:16].N>>[NH2:18][CH:14]([C:8]1[C:9]([Cl:13])=[CH:10][CH:11]=[CH:12][C:7]=1[Cl:6])[C:15]([NH2:17])=[O:16]Participants
4
Procedure
To a stirred and cooled amount of 450 g of concentrated sulfuric acid there were added 23 g of intermediate (2). Stirring was continued overnight at room temperature. The reaction mixture was poured into 2000 g of ice-water and the whole was basified with ammonia. The product was extracted with trichloromethane and the extract was dried, filtered and evaporated. The residue was crystallized from 240 g of 2-propanol at -20° C. The product was filtered off, washed with 2-propanol and petroleumether and dried, yielding 13.5 g of (±)-α-amino-2,6-dichlorobenzeneacetamide; mp. 166.3° C. (interm. 3).
Workup
- stirringStirring
- extractionThe product was extracted with trichloromethane
- customthe extract was dried
- filtrationfiltered
- customevaporated
- customThe residue was crystallized from 240 g of 2-propanol at -20° C
- filtrationThe product was filtered off
- washwashed with 2-propanol and petroleumether
- customdried
Sources & evidence
- ORD record
- ord-4b7fb40a6de74cbb8f5b8ebafcc8c1c8
- Source dataset
- uspto-grants-1997_02
- Patent number
- US05604230
Reaction notes
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