Butylamine → HCID 135623127, compound
Reaction equation
[OH:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][CH:5]=[CH:4][C:3]=1[C:10](=O)[CH2:11][S:12]([CH3:14])=[O:13].[CH2:16]([NH2:20])[CH2:17][CH2:18][CH3:19]>>[CH2:16]([N:20]=[C:10]([C:3]1[CH:4]=[CH:5][CH:6]=[C:7]([O:8][CH3:9])[C:2]=1[OH:1])[CH2:11][S:12]([CH3:14])=[O:13])[CH2:17][CH2:18][CH3:19]Participants
3
Procedure
A solution of 2'-hydroxy-3'-methoxy-2-(methylsulfinyl)acetophenone (5 g, 0.022 mole) in n-butylamine (25 ml) was stirred at room temperature for 24 hrs. The reaction mixture was poured into petroleum ether (200 ml) and the product, which precipitated, was filtered off. Recrystallization from ethylacetate gave yellow crystals (6.0 g, 97%), mp 125°-127°.
Workup
- customthe product, which precipitated
- filtrationwas filtered off
- customRecrystallization from ethylacetate
Sources & evidence
- ORD record
- ord-cf8129365b33409db43e561439b4dbb8
- Source dataset
- uspto-grants-1977_08
- Patent number
- US04039579
Reaction notes
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