4-Toluenesulfonyl chloride → HCID 19771312, compound
Reaction equation
[CH3:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([N+:10]([O-:12])=[O:11])[C:3]=1[CH2:4][OH:5].[S:13](Cl)([C:16]1[CH:22]=[CH:21][C:19]([CH3:20])=[CH:18][CH:17]=1)(=[O:15])=[O:14].C1(NC2CCCCC2)CCCCC1>CC(C)=O>[S:13]([C:16]1[CH:22]=[CH:21][C:19]([CH3:20])=[CH:18][CH:17]=1)([O:5][CH2:4][C:3]1[C:6]([N+:10]([O-:12])=[O:11])=[CH:7][CH:8]=[CH:9][C:2]=1[CH3:1])(=[O:15])=[O:14]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A 100 mL round bottomed flask equipped with a dropping funnel was charged with 2.50 g of 2-methyl-6-nitrobenzyl alcohol and 3.14 g of tosyl chloride dissolved in 30 mL of dry acetone under argon. To the mixture was added dropwise 3.30 mL of dicylohexylamine dissolved in 5 mL of dry acetone while cooling so as to keep the temperature below 15° C. The reaction mixture was brought to room temperature and stirred for 1 day. The mixture was filtered to remove dicyclohexylamine hydrochloride, the solvent removed under vacuum, and the residue chromatographed over silica gel using carbon tetrachloride as the eluent. The product was recrystallized from methylene chloride/pentane to give 1.82 g (38% yield) of white crystals.
Workup
- customA 100 mL round bottomed flask equipped with a dropping funnel
- temperaturewhile cooling so as
- customthe temperature below 15° C
- customwas brought to room temperature
- filtrationThe mixture was filtered
- customto remove dicyclohexylamine hydrochloride
- customthe solvent removed under vacuum
- customthe residue chromatographed over silica gel
- customThe product was recrystallized from methylene chloride/pentane
Sources & evidence
- ORD record
- ord-a6031744064947e68f3b36e0be9a9a8c
- Source dataset
- uspto-grants-1992_08
- Patent number
- US05135838
Reaction notes
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