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Cyclohexanone → N-cyclohexylidene-2-methylpropane-2-sulfinamide

HRID 1160140
Notes
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Reaction equation

HRID 1160140 reaction equation
[C:1]1(=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:8]([S@@:12]([NH2:14])=[O:13])([CH3:11])([CH3:10])[CH3:9].C(=O)(O)[O-].[Na+]>C1COCC1.[O-]CC.[O-]CC.[O-]CC.[O-]CC.[Ti+4]>[C:1]1(=[N:14][S:12]([C:8]([CH3:11])([CH3:10])[CH3:9])=[O:13])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 7967CyclohexanoneHCID 516892Sodium BicarbonateHCID 11355477tert-Butylsulfinamide, (S)-(-)-

Product 1

HCID 58591374N-cyclohexylidene-2-methylpropane-2-sulfinamideYield 76.1%

Reagents, catalysts & solvents 2

HCID 76524Titanium tetraethoxideCatalyst
HCID 8028
Tetrahydrofuran
Solvent
2×

Conditions

Temperature
60 °C

Procedure

Titanium tetraethoxide (2 eq, 3.56 mL, d 1.088) was added to a solution of cyclohexanone (1.2 eq, 1.0 g, 1.05 mL, d 0.947) in 20 mL of dry THF under nitrogen atmosphere. After 5 min, (S)-t-butanesulfinamide (1200-A, 1.028 g) in 10 mL of THF was added dropwise. The mixture was heated to 60° C. overnight. The reaction mixture was poured into an equal volume of aqueous saturated sodium bicarbonate solution with rapid stirring and immediately filtered through celite. The filter cake was washed with ethyl acetate (50 mL). The layers in the filtrate were separated and the aqueous layer was extracted with ethyl acetate (30 mL). The combined organic layers were dried over magnesium sulfate, filtered and concentrated. The residue was chromatographed on silica gel (gradient:ether/hexanes; 1:9 to 1.1) to afford the product 1200-B (1.3 g; 76%) as a colorless oil. The product was kept under inert atmosphere at −20° C.

Workup

  1. filtrationimmediately filtered through celite
  2. washThe filter cake was washed with ethyl acetate (50 mL)
  3. customThe layers in the filtrate were separated
  4. extractionthe aqueous layer was extracted with ethyl acetate (30 mL)
  5. dry with materialThe combined organic layers were dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was chromatographed on silica gel (gradient:ether/hexanes; 1:9 to 1.1)

Sources & evidence

ORD record
ord-bc87b062ebe54a9391f9c6a5e09687aa
Source dataset
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07816326B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes