Sodium Carbonate → HCID 13827675, compound
Reaction equation
[CH2:1]([NH:8][OH:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:10]1([CH2:18]Br)[CH:15]=[CH:14][C:13]([CH2:16]Br)=[CH:12][CH:11]=1.C(=O)([O-])[O-].[Na+].[Na+]>>[OH:9][N:8]([CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[CH2:18][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][N:8]([OH:9])[CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:12][CH:11]=1Participants
4
Procedure
The procdure of Example 1 is repeated using 5.59 g of benzylhydroxylamine, 5.99 g of p-xylylene dibromide and 6.0 g of anhydrous sodium carbonate. The reaction product is recrystallized from acetonitrile to give the product as a white solid; m.p. 160°-163° C.
Workup
- customThe reaction product is recrystallized from acetonitrile
Sources & evidence
- ORD record
- ord-52111a3ec5fb4c96bd25605a70d3b7ea
- Source dataset
- uspto-grants-1987_03
- Patent number
- US04649221
Reaction notes
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