Trityl chloride → HCID 15127968, compound
Reaction equation
[CH2:1]([OH:6])[CH:2]([OH:5])[CH2:3][CH3:4].[C:7]1([C:13](Cl)([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>N1C=CC=CC=1.CCOC(C)=O.O>[C:13]([O:6][CH2:1][CH:2]([OH:5])[CH2:3][CH3:4])([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)([C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 100 °C
Procedure
To a solution of 1,2-butandiol (2 g) in anh. pyridine (15 mL) was added triphenylmethyl chloride (8 g). The dark reaction mixture was heated at 100° C. for 8 hr and stirred at r.t. for 18 hr. The mixture was then poured in EtOAc/H2O, the phases were separated and the organic layer was washed with sat. aq. NaCl and dried over Na2SO4. The solids were filtered and the solvent evaporated. The residual pyiridine was eliminated by filtration through a pad of silica gel (cHex/EtOAc 8/2). The solvent was evaporated and the residue was purified by flash chromatography (silica gel, cHex/EtOAc 95:5) to give the title compound (2.67 g)
Workup
- customThe dark reaction mixture
- customthe phases were separated
- washthe organic layer was washed with sat. aq. NaCl
- dry with materialdried over Na2SO4
- filtrationThe solids were filtered
- customthe solvent evaporated
- filtrationThe residual pyiridine was eliminated by filtration through a pad of silica gel (cHex/EtOAc 8/2)
- customThe solvent was evaporated
- customthe residue was purified by flash chromatography (silica gel, cHex/EtOAc 95:5)
Sources & evidence
- ORD record
- ord-d09a6532bf344b7ab25fae1eca002e6c
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07462622B2
Reaction notes
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