1,2-Dichloroethane → Cinnamoylbenzene
Reaction equation
[C:1]([OH:4])(=O)[CH3:2].[C:5](O)(=O)C.C(O)(=O)C.C(O)(=O)C.[CH:17]1([CH2:28][N+]([O-])=O)O[C@H:24]([CH2:26]O)[C@@H:22](O)[C@H:20](O)[C@H:18]1O.[C:32]1(N=C=O)[CH:37]=[CH:36]C=[CH:34][CH:33]=1.ClCCCl.C(N(CC)CC)C>>[C:17]1([CH:28]=[CH:5][C:1]([C:2]2[CH:36]=[CH:37][CH:32]=[CH:33][CH:34]=2)=[O:4])[CH:26]=[CH:24][CH:22]=[CH:20][CH:18]=1Participants
Conditions
- Temperature
- 78 °C
Procedure
To a solution of 44 mg (0.11 mmol) a D-glucopyranosylnitromethane tetra-acetate (alpha anomer) and 24 μL (0.22 mmol) phenyl isocyanate in 0.80 mL 1,2-dichloroethane containing 30 mg (0.016 mmol) Rink Amide Resin bound compound 1, 2 mL (0.016 mmol) triethylamine was added under argon. The mixture was refluxed and shaken at 78° C. for 15 hours. It was allowed to cool down to room temperature. The resin bound compound 2 was collected in a 3 mL filtering column and was washed with N,N-dimethylformamide (3×2 mL), methylene chloride (3×2 mL) and dried under vacuum. The dried Resin bound compound 2 was treated with 2 mL 20% trifluoroacetic acid in methylenechloride for 20 minutes. The solid was filtered off and washed 3 times with 1.5 mL methylene chloride. The combined washings were concentrated and dried under vacuum to give 12 mg product 3 of ca. 95% purity. The spectral data consisted of: Electrospray MS m/z 884 (M+ +1). ##STR60##
Workup
- additionwas added under argon
- temperatureThe mixture was refluxed
- temperatureto cool down to room temperature
- customwas collected in a 3 mL
- filtrationfiltering column
- washwas washed with N,N-dimethylformamide (3×2 mL), methylene chloride (3×2 mL)
- customdried under vacuum
- additionwas treated with 2 mL 20% trifluoroacetic acid in methylenechloride for 20 minutes
- filtrationThe solid was filtered off
- washwashed 3 times with 1.5 mL methylene chloride
- concentrationThe combined washings were concentrated
- customdried under vacuum
Sources & evidence
- ORD record
- ord-d38de36018e94ab5959668752e47d8c1
- Source dataset
- uspto-grants-1999_09
- Patent number
- US05958792
Reaction notes
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