Trifluoroacetic acid → HCID 67672704, compound
Reaction equation
[C@H:1]1([NH2:8])[CH2:6][CH2:5][CH2:4][C@H:3]([NH2:7])[CH2:2]1.[F:9][C:10]([F:15])([F:14])[C:11]([OH:13])=[O:12]>>[F:9][C:10]([F:15])([F:14])[C:11]([OH:13])=[O:12].[C@H:1]1([NH2:8])[CH2:6][CH2:5][CH2:4][C@H:3]([NH2:7])[CH2:2]1Participants
3
Procedure
±-trans-Cyclohexane-1,3-diamine: 22.9 g of the BOC derivative are introduced into 1 00 ml of trifluoroacetic acid while cooling with ice. The mixture is left at RT for 4 hours, evaporated and the residue is recrystallized from 200 ml of acetonitrite. 8.5 g of ±-trans-cyclohexane-1,3-diamine trifluoroacetate, m.p. 200° C. (sintering) are obtained.
Workup
- temperaturewhile cooling with ice
- customevaporated
- customthe residue is recrystallized from 200 ml of acetonitrite
Sources & evidence
- ORD record
- ord-ffc6130b383646acb455c97c1240bde5
- Source dataset
- uspto-grants-1998_04
- Patent number
- US05736557
Reaction notes
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