Dimethyl Sulfide → 2-Amino-3-(methylthiomethyl)benzotrifluoride

HRID 326990Notes

Reaction equation

HRID 326990 reaction equation
[CH3:1][S:2][CH3:3].[F:4][C:5]([F:14])([F:13])[C:6]1[CH:12]=[CH:11][CH:10]=[CH:9][C:7]=1[NH2:8].ClN1C(=O)CCC1=O.C(N(CC)CC)C>C(Cl)Cl>[CH3:1][S:2][CH2:3][C:9]1[CH:10]=[CH:11][CH:12]=[C:6]([C:5]([F:4])([F:14])[F:13])[C:7]=1[NH2:8]

Participants

6

Conditions

Temperature
15 °C

Procedure

Dimethylsulfide, 16 ml, was syringed all at once into a solution of 25.0 grams (g) of 2-(trifluoromethyl)aniline in 400 milliliters (ml) of methylene chloride. The reaction solution was cooled to 15° C. and 29.0 g of N-chlorosuccinimide was added in small portions over a 20 minute period at such a rate that the reaction temperature did not exceed 20° C. The reaction mixture was stirred at 15° C. for 15 minutes, then 30.4 ml of triethylamine was added dropwise over 15 minutes at such a rate that the temperature did not exceed 15° C. After an additional five minutes of stirring, the reaction was refluxed overnight, allowed to cool to room temperature, washed with two 200 ml portions of 10% sodium hydroxide, the organic phase separated, dried with magnesium sulfate and filtered. The remainder of the solvent was distilled off to yield 35.8 g of the crude desired product which was used without any additional purification in subsequent reactions.

Workup

  1. customdid not exceed 20° C
  2. customdid not exceed 15° C
  3. stirringAfter an additional five minutes of stirring
  4. temperaturethe reaction was refluxed overnight
  5. temperatureto cool to room temperature
  6. washwashed with two 200 ml portions of 10% sodium hydroxide
  7. customthe organic phase separated
  8. dry with materialdried with magnesium sulfate
  9. filtrationfiltered
  10. distillationThe remainder of the solvent was distilled off

Sources & evidence

ORD record
ord-9bd097b9552242febf8008a8323bf7ca
Source dataset
uspto-grants-1993_12
Patent number
US05272128

Reaction notes

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