1-Adamantanecarbonyl chloride → Decane
Reaction equation
C([NH+]([CH2:6][CH3:7])CC)C.[C:8]12(C(Cl)=O)C[CH:12]3[CH2:13][CH:14](C[CH:10]([CH2:11]3)[CH2:9]1)[CH2:15]2>C(#N)C.N1C=CC=CC=1>[CH3:14][CH2:15][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:6][CH3:7]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The dimethoxytrityl group of the derivatized CPG from Example 9 is removed by a treatment with 2% dichloroacetic acid followed by washing with dry acetonitrile. The CPG is washed with acetonitrile-pyridine (1:1) followed by a simultaneous treatment of the CPG with 10 to 30 equivalents of the 10-O-(dimethoxytrityl)decyl-phosphonic acid as the triethylammonium salt, 20-30 equivalents of adamantane carbonyl chloride in acetonitrile-pyridine. The CPG is then washed with acetonitrile-pyridine and then treated with diisopropyl phosphite adamantane carbonyl chloride (0.2M) to cap all unreacted hydroxyl groups. Finally, the CPG is washed with acetonitrile/pyridine 1:1 and then acetonitrile. An estimate of coupling efficiency is derived from the treatment of the CPG with dichloracetic acid in acetonitrile followed by a measurement of the absorbance of an aliquot at 498 nm. Repeating the above procedure n times will yield an oligomer with n+1 decane units and n H-phosphonate linkages. The oligomer is tethered to a LCAA CPG by a succinate group as described above.
Workup
- customThe dimethoxytrityl group of the derivatized CPG from Example 9 is removed by a treatment with 2% dichloroacetic acid
- washby washing with dry acetonitrile
- washThe CPG is washed with acetonitrile-pyridine (1:1)
- washThe CPG is then washed with acetonitrile-pyridine
- additiontreated with diisopropyl phosphite adamantane carbonyl chloride (0.2M)
- customto cap all unreacted hydroxyl groups
- washFinally, the CPG is washed with acetonitrile/pyridine 1:1
Sources & evidence
- ORD record
- ord-42eeddfbee7d4200978cf6cca485c302
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05717083
Reaction notes
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