Dichloromethane → (NE,R)-2-methyl-N-[[4-[4-(trifluoromethyl)phenyl]phenyl]methylidene]propane-2-sulfinamide

HRID 2406916Notes

Reaction equation

HRID 2406916 reaction equation
[F:1][C:2]([F:18])([F:17])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([CH:15]=O)=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.[CH3:19][C:20]([S@:23]([NH2:25])=[O:24])([CH3:22])[CH3:21].ClCCl.C(=O)(O)[O-].[Na+]>[O-]CC.[Ti+4].[O-]CC.[O-]CC.[O-]CC.[Ti].CO>[CH3:19][C:20]([S@:23](/[N:25]=[CH:15]/[C:12]1[CH:13]=[CH:14][C:9]([C:6]2[CH:7]=[CH:8][C:3]([C:2]([F:18])([F:17])[F:1])=[CH:4][CH:5]=2)=[CH:10][CH:11]=1)=[O:24])([CH3:22])[CH3:21]

Participants

8

Procedure

A round bottom flask equipped with a condenser was charged with 4′-(trifluoromethyl)biphenyl-4-carbaldehyde (20.0 g, 79.9 mmol), (R)-(+)-2-methylpropane-2-sulfinamide (9.69 g, 79.9 mmol) and dichloromethane (400 mL). Titanium(IV) ethoxide (33.2 mL, 160 mmol) was then added, and the mixture was heated to reflux for 3 hours. Methanol (50 mL) and saturated sodium bicarbonate (10 mL) were then added to the reaction, causing the titanium salts to precipitate. This mixture was stirred for 30 minutes and then filtered, rinsing with ethyl acetate. Sodium sulfate was added to the filtrate to remove the water and then filtered a second time. The solvent was removed under reduced pressure to afford (R,E)-2-methyl-N-((4′-(trifluoromethyl)biphenyl-4-yl)methylene)propane-2-sulfinamide (23.7 g, 84%) as a white solid. 1H NMR (400 MHz, CDCl3, δ): 1.30 (s, 9 H) 7.70-7.74 (m, 2 H) 7.74 (s, 4 H) 7.95-7.99 (m, 2 H) 8.66 (s, 1 H). MS (M+1): 354.1.

Workup

  1. customA round bottom flask equipped with a condenser
  2. temperaturethe mixture was heated
  3. temperatureto reflux for 3 hours
  4. customto precipitate
  5. filtrationfiltered
  6. washrinsing with ethyl acetate
  7. additionSodium sulfate was added to the filtrate
  8. customto remove the water
  9. filtrationfiltered a second time
  10. customThe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-c97af1219b0141c39e6c8155fb96b223
Source dataset
uspto-grants-2014_08
Patent number
US08809342B2

Reaction notes

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