Dimethyl Sulfoxide → HCID 86584165, compound
Reaction equation
CS(C)=O.[C:5](Cl)(=[O:9])[C:6](Cl)=[O:7].C(NCCCO)(O[CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=O.P([O-])(O)(O)=[O:27].[K+].[CH2:32]([N:34]([CH2:37]C)CC)C>C(Cl)Cl>[C:32](=[N:34][CH2:37][CH:5]([O:9][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH:6]=[O:7])=[O:27]Participants
Conditions
- Temperature
- -48 °C
Procedure
335 mL of dimethylsulfoxide and 9 L of methylene chloride were combined and chilled to −48° C. 313 mL of oxalyl chloride was added over 25 minutes so that the temperature remained below −40° C. Cooled to −48° C., and added 500 grams of N-Cbz-3-amino-1-propanol dissolved in 1 L of methylene chloride so that the temperature remained below −40° C. Stirred for an additional hour at −45° C. 1325 mL of triethylamine was added at such a rate that the temperature remained below −40° C. After stirring an additional 15 minutes at −40° C., the mixture was allowed to warm to −30° C., then added 2:5 L of 20% aqueous potassium dihydrogen phosphate. Stirred for one hour, then separated the layers, washed the organic layer with brine, and dried with magnesium sulfate. The resulting aldehyde was kept in solution at −20° C. until needed.
Workup
- customremained below −40° C
- temperatureCooled to −48° C.
- customremained below −40° C
- customremained below −40° C
- stirringAfter stirring an additional 15 minutes at −40° C.
- temperatureto warm to −30° C.
- additionadded 2
- stirringStirred for one hour
- customseparated the layers
- washwashed the organic layer with brine
- dry with materialdried with magnesium sulfate
- customwas kept in solution at −20° C.
Sources & evidence
- ORD record
- ord-eaf9240b6afe4862a88fd2e2758fecd8
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06313296B1
Reaction notes
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