Pivaloyl chloride → HCID 20533876, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH3:10].[C:11](Cl)(=[O:16])[C:12]([CH3:15])([CH3:14])[CH3:13]>>[C:11]([NH:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH3:10])(=[O:16])[C:12]([CH3:15])([CH3:14])[CH3:13]Participants
3
Procedure
1-Amino-2-(2-methylphenyl)ethane and pivaloyl chloride were reacted in the same way as in step (a) of Example 1 to afford 1-pivaloylamino-2-(2-methylphenyl)-ethane. The product was successively reacted in the same way as in steps (b), (c), (d) and (e) of Example 1 to afford 1-tert-butylsioquinoline-5-acetonitrile.
Sources & evidence
- ORD record
- ord-2c1ae988de6c4476957b16948696cd41
- Source dataset
- uspto-grants-1982_06
- Patent number
- US04337256
Reaction notes
Loading…