Water → HCID 86742222, compound
Reaction equation
[Cl:1][C:2]1[C:15]([Cl:16])=[C:14](/[CH:17]=[C:18](/[N+:21]([O-:23])=[O:22])\[CH2:19][CH3:20])[CH:13]=[CH:12][C:3]=1[O:4][C:5]1([C:9]([OH:11])=[O:10])[CH2:8][CH2:7][CH2:6]1.O.C(=O)(O)[O-].[Na+:29]>>[Cl:1][C:2]1[C:15]([Cl:16])=[C:14](/[CH:17]=[C:18](/[N+:21]([O-:23])=[O:22])\[CH2:19][CH3:20])[CH:13]=[CH:12][C:3]=1[O:4][C:5]1([C:9]([O-:11])=[O:10])[CH2:8][CH2:7][CH2:6]1.[Na+:29]Participants
4
Procedure
250 mg of (E)-1-[2,3-dichloro-4-(2-nitro-1-butenyl)phenoxy]cyclobutane-1-carboxylic acid is dissolved in 31 ml of 0.1 N sodium bicarbonate and sufficient isotonic buffer to make a final volume of 100 ml. The water from all sources was pyrogen-free. The solution is sterilized by filtration.
Workup
- filtrationThe solution is sterilized by filtration
Sources & evidence
- ORD record
- ord-3d4384e6247d4481a1868f3913bc6e85
- Source dataset
- uspto-grants-1988_06
- Patent number
- US04751244
Reaction notes
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