Diisopropylethylamine → 2-(Decylthio)acetaldehyde

Temperature

-40 °C

Under nitrogen, 2-(decylthio)ethanol (50 g, 230 mmol), N,N-diisopropylethylamine (128 ml, 730 mmol) and methylene chloride (400 ml) were cooled to −40° C. To this solution was added, over 15 minutes, a solution of sulfur trioxide pyridine complex (116 g, 730 mmol) in dimethyl sulfoxide (600 ml) and methylene chloride (200 ml). After addition, the mixture was stirred a further 15 minutes at −40° C., then 600 ml ice water as added. The mixture was removed from the cooling bath, 1 L water was added, and the liquids partitioned. The organic phase was washed with 1 L of 1 N hydrochloric acid, and dried over magnesium sulfate. Filtration gave 600 ml liquid, which was diluted with 600 ml hexane and passed through 200 ml silica. The silica was washed with 100 ml 50% methylene chloride/hexane, then 300 ml methylene chloride. The combined organics were concentrated in vacuo to give 2-decylthio)acetaldehyde (48 g, 220 mmol) as a colorless liquid that was used without further purification.

1. additionTo this solution was added, over 15 minutes
2. additionAfter addition
3. customThe mixture was removed from the cooling bath, 1 L water
4. additionwas added
5. customthe liquids partitioned
6. washThe organic phase was washed with 1 L of 1 N hydrochloric acid
7. dry with materialdried over magnesium sulfate
8. filtrationFiltration

ORD record

ord-f8e510d7cf624d16baed89d7d29dbfc5

Source dataset

uspto-grants-2007_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07208471B2