Ammonium thiocyanate → 2-(4-Fluorophenyl)acetyl isothiocyanate

HRID 1047455Notes

Reaction equation

HRID 1047455 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9](Cl)=[O:10])=[CH:4][CH:3]=1.[S-:12][C:13]#[N:14].[NH4+]>CC#N>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([N:14]=[C:13]=[S:12])=[O:10])=[CH:4][CH:3]=1

Participants

4

Conditions

Temperature
50 °C

Procedure

To a solution of crude 1a (27.4 g, 159 mmol) from the previous step in MeCN (159 mL) was added ammonium thiocyanate (12.69 g, 167 mmol, 1.05 eq.). The fine yellow slurry was heated at 50° C. for 1 h. After cooling down to 0° C., the reaction mixture was filtered through a Celite pad and the cake was washed with MeCN (10 mL). The filtrate and washings were combined and concentrated to a volume of 30-40 mL, cooled again to 0° C. and filtered through a Celite pad. The cake was washed with MeCN (10 mL). The filtrate and washings were combined and concentrated to the same volume of 30-40 mL. The resultant solution contained 2-(4-fluorophenyl)acetyl isothiocyanate (2, assumed quantitative yield, Method B). Half of this solution was used in the next step.

Workup

  1. temperatureAfter cooling down to 0° C.
  2. filtrationthe reaction mixture was filtered through a Celite pad
  3. washthe cake was washed with MeCN (10 mL)
  4. concentrationconcentrated to a volume of 30-40 mL
  5. temperaturecooled again to 0° C.
  6. filtrationfiltered through a Celite pad
  7. washThe cake was washed with MeCN (10 mL)
  8. concentrationconcentrated to the same volume of 30-40 mL

Sources & evidence

ORD record
ord-171a27456a2142d3b5e7592731e7799d
Source dataset
uspto-grants-2013_10
Patent number
US08569503B2

Reaction notes

Loading…