Reaction equation
C(N(CC)CC)C.[N+](=[C:10]1[CH:19]=[CH:18][C:17]2[C:16](S(Cl)(=O)=O)=[CH:15][CH:14]=[CH:13][C:12]=2[C:11]1=O)=[N-]>CN(C)C1C=CN=CC=1.C(Cl)Cl>[CH:12]12[CH2:11][CH:15]([CH2:14][CH2:13]1)[CH:16]1[CH:17]2[CH2:18][CH2:19][CH2:10]1Participants
Conditions
- Temperature
- 25 °C
Procedure
To a solution of 1.86 g 4,8-Bis(hydroxyeth-1'-yl)tricyclo [5.2.1.02,6 ] decane, 0.93 g of 4-di-methylamino-pyridine, 4.7 ml of triethylamine and 30 ml of CH2Cl2 at 0° C. was added a solution of 7.8 g of 6-diazo-5,6-dihydro-5-oxo-1-naphthalene sulfonyl chloride and 80 ml of methylene chloride over 0.5 hr. The mixture was stirred 1/2 hour at 9° C. and 6 hours at 25° C. and then diluted with 100 ml of methylene chloride. The mixture was then filtered and the methylene chloride phase washed with 100 ml of 10% sodium bicarbonate solution, 100 ml of water, 100 ml of 2 N sulfuric acid solution 50 ml of 5% sodium bicarbonate solution and 50 ml of water. The solution was then dried over sodium sulfate and the solvent removed at reduced pressure to give 3.5 g of product.
Workup
- filtrationThe mixture was then filtered
- washthe methylene chloride phase washed with 100 ml of 10% sodium bicarbonate solution, 100 ml of water, 100 ml of 2 N sulfuric acid solution 50 ml of 5% sodium bicarbonate solution and 50 ml of water
- dry with materialThe solution was then dried over sodium sulfate
- customthe solvent removed at reduced pressure
Sources & evidence
- ORD record
- ord-c30b13df8d8d43868ce742d1f051f00a
- Source dataset
- uspto-grants-1983_08
- Patent number
- US04397937
Linked notes
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